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Saudi Aramco
THE SAUDI ARAMCO JOURNAL OF TECHNOLOGY
Journal of Technology
A quarterly publication of the Saudi Arabian Oil Company
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The Saudi Aramco Journal of Technology is EDITORIAL ADVISORS (CONTINUED) PRODUCTION COORDINATION
published quarterly by the Saudi Arabian Oil
Company, Dhahran, Saudi Arabia, to provide Omar S. Al-Husaini Richard E. Doughty
the company’s scientific and engineering General Manager, Drilling & Workover Operations
communities a forum for the exchange of DESIGN
Waleed A. Al-Mulhim
ideas through the presentation of technical
information aimed at advancing knowledge
Chief Petroleum Engineer Graphic Engine Design Studio,
in the hydrocarbon industry. Austin, Texas, U.S.A.
Ammar A. Al-Nahwi
Manager, Research and Development Center
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Spring 2019
Saudi Aramco
THE SAUDI ARAMCO JOURNAL OF TECHNOLOGY
Journal of Technology
A quarterly publication of the Saudi Arabian Oil Company
Contents
ABSTRACT demand. Some of these additives and products are not eco-
friendly and therefore have serious limitations in their appli-
The oil and gas industry has a long-standing initiative to cations, due to their detrimental impact on the surrounding
develop and use the most environmental solutions in the environments, including ecosystems, habitats, water resources,
exploration and recovery of oil and gas resources. As part of farming lands, the local population, and rig site workers,
this continual effort, research is ongoing to create eco-friend- etc.1-3.
ly, virtually nontoxic and readily biodegradable base fluids, That’s why the regional, federal and global environmental
lubricants, and emulsifiers to successfully complete drilling agencies are enacting increasingly strict environmental rules
and completion requirements, without causing any damage to and regulations to safeguard the local, regional, and global
the environment or other resources. environments, and also to avoid any short- and long-term
There is a significant volume of waste vegetable oil (WVO) detrimental impact on marine and terrestrial resources, hab-
generated by the food and catering industry, which has no itats, population, etc. Due to the concern of the global com-
aromatic oil content, is virtually nontoxic, and readily bio- munities, the industry has realized the need for a replacement
degradable, and therefore, can be a potential source for the for the non-eco-friendly additives and fluids — to be in the
development of eco-friendly base fluids, lubricants, emulsifi- forefront of the best drilling practices. There is an expected
ers, and spotting fluids to be in the forefront of best drilling annual growth of 7% to 10% of eco-friendly lubricants in the
practices. This article describes a set of newly developed green U.S. market over the next few years, compared to an overall
mud additives that have been synthesized using waste cooking 2% growth rate of conventional lubricants. This is reflected
oil generated by the food and catering industry. Recycling of in the increasing research to develop green additives and base
the waste cooking oil not only provides a technical solution fluids to replace or reduce the use of less eco-friendly additives
for the oil and gas industry, but also addresses the disposal and products3, 4-6.
problems of the food and catering industry. Currently, many countries of the world have prohibited the
Experimental results demonstrating the various applications use of non-eco-friendly additives and fluids in environmentally
of the newly developed green products indicate similar or sensitive areas, to prevent damage and degradation of the
better performance compared to the commercially available environment and surrounding ecosystems. The operating com-
equivalent products used by the oil and gas industry. Subse- panies all over the world take extra care to avoid any damage
quently, the newly developed products are viable alternatives and degradation of the environment by introducing new
for some of the imported non-eco-friendly or less eco-friendly products in the market and providing well-defined operational
oil-based products, used for exploration and exploitation of guidelines. In spite of strict operational guidelines, accidental
oil and gas resources. Due to the replacement of equivalent spills, leakage and discharge of any less eco-friendly products
imported products, these locally developed products will sig- in the surrounding environment can cause environmental
nificantly reduce the mud additive import cost. Also, due to damage and pollution to the water systems, farming land, top
the eco-friendly nature of these products, they will help in the soil, coastal areas, etc. Therefore, identification of a better
exploration and exploitation of oil and gas resources without alternative is always encouraged by the industry.
causing any negative impact on other marine and terrestrial The oil-based muds (OBMs) leaked or disposed after wash-
resources. ing the mud tanks, mud pumps, and flow lines, may travel
into the surrounding ecosystems, water reserves, subsurface
INTRODUCTION water table, etc., and can cause serious contamination due
to the incorporation of benzene-like toxins in the surface
The oil and gas industry uses various types of chemicals and subsurface water system. Its detrimental impact — both
and additives to design various fluid systems to explore and on the soil and drinking water — could be a serious health
exploit hydrocarbon resources to meet the global energy hazard for the surrounding environment, habitats, and
120
75
PV (cP)PV (cP)
50
food debris from the waste cooking oil. After physical treat-
ment, chemical modification was done by water hydrolysis
25
and methanol (CH3OH) esterification to improve the viscous
characteristics, low temperature flow behavior, and interface 25
infiltration characteristics. Figures 1 and 2 show the two
chemical modification methods used and the reaction products
0
generated by the interactions. Figure 1 shows esterification us- MO VO RVO WVO RWVO SAO
ing CH3OH and sodium hydroxide (NaOH), and Fig. 2 shows 0
Fig. 4. PV values
MO of MO, VO
VO, RVO, WVO,
RVO RWVO,WVO
and SAO. RWVO SAO
a chemical modification using water and NaOH.
Fig.
Fig. 4.
4. PV
PVvalues
valuesofofMO,
MO,VO,
VO,RVO, WVO,
RVO, RWVO,
WVO, and SAO.
RWVO, and SAO.
GREEN PRODUCTS
15
PV Ratio
base stocks were also used to assess their suitability as lubri- 10
PV Ratio
cants, to reduce the frictional resistance of water-based muds
5
(WBMs) and emulsifiers, to create a stable and tight emulsion
5
in invert emulsion mud systems. A detailed description of the
experimental results along with the interpretation of the data 0
are given next. WVO/MO VO/MO RWVO/MO RVO/MO
0
WVO/MO VO/MO RWVO/MO RVO/MO
Fig. 5.
Fig. 5. PV
PV ratios
ratiosofofVO,
VO,RVO,
RVO, WVO,
WVO, RWVO
RWVO withwith respect
respect toPV
to the thevalue
PV value
of theofMO.
the
Eco-Friendly Base Stock MO.
Fig. 5. PV ratios of VO, RVO, WVO, RWVO with respect to the PV value of the MO.
The esterification process provided an eco-friendly base stock base stock, it will provide an OBM system with environmental
with viscous characteristics similar to mineral, diesel, and a characteristics similar to WBM systems.
As a base
highly refined Saudi Arabian NaOH
oil (SAO) widely used aslubricant the for
oil, and as a The comparison of plastic viscosity (PV) values of the MO
CH OH 3
base stocks for conventional OBM development. Figure water-based shown in Fig. 4 with the PV values of VO, refined VO (RVO),
mud.3
60 °C, 6 hours
shows the rheological profile (viscous characteristics) of the WVO, RWVO, and SAO indicate extremely high PV values
original
Glycerol
WVO and WVO ester produced after chemical modi-
Triglyceride Methyl Ester of Fatty Acid for VO and WVO with respect to the PV value of the MO,
fication,
Fig. 1. Diagramalong with
showing the themodification
chemical rheological profiles
of WVO using CH3OH ofand diesel
NaOH. and MO.
but close PV values for the RVO and RWVO. This indicates
The data clearly indicates very high viscous characteristics for that the original VO and WVO are not suitable for a func-
the WVO. That’s why the as received WVO is not suitable tional OBM formulation, due to excessive PV values. After
for development of an NaOH
H OOBM system with desirable mud
Emulsifer prop-
for chemical modification, these oils have PV values close to the
2 invert emulsion
erties. After chemical processing, the refined WVO (RWVO) oil-based mud. MO’s PV, and is thereby suitable for OBM formulations.
60 °C, 6 hours
shows a viscous profile very similar to the viscous profiles of Figure 5 shows the analyses of the PV ratios of VO and
Triglyceride Glycerol Fatty Acid
diesel and MOs. This indicates its suitability to use as a base MO, WVO and MO, RVO and MO, and RWVO and MO.
stock
Fig. for showing
2. Diagram a newthegeneration of OBM
chemical modification development
of WVO using water and NaOH. with techni- The data indicates more than 11 times higher PV ratios for
cal performance similar or equivalent to the conventional die- the as received VO and WVO, but less than 1.5 PV ratios for
sel and mineral OBMs. Due to the eco-friendly nature of the the RVO and RWVO. This again demonstrates the suitability
160 of the chemically modified VO and WVO for developing
Mineral Oil WVO SAO RWVO
a new generation of OBM systems with superior environ-
120
mental properties. The marginally higher PV values of RVO
Dial Reading
Fig.
Fig.3.3.
Rheological profiles
Rheological of the MO,
profiles of WVO, SAO,WVO,
the MO, and RWVO-based
SAO, and base fluid.
RWVO-based base fluid.
An eco-friendly RWVO OBM with a 70/30 oil-water ratio
PV (cP)
YP PV
50
60 bentonite mud from 0.344 to 0.126 — an approximate 63%
(cP)
40 YP PV
) and
50
reduction of the COF value of the original bentonite mud.
ft2) andft2PV 30
40
Comparison of the lubricating performance of the ARC Eco-
YP (lb/100
20
30
10 Lube with respect to the commercial green lubricant (CGL)
YP (lb/100
20
0
10 SAO Mud (RT) SAO Mud SAO Mud WVO Mud (RT) WVO Mud WVO Mud indicates somewhat better performance for the ARC Eco-Lube
(120 °F) (250 °F) (120 °F) (250 °F)
0
SAO Mud (RT) SAO Mud Drilling
SAO Mud Fluid Systems
WVO Mud (RT) WVO Mud WVO Mud
with respect to the CGL.
(120 °F) (250 °F) (120 °F) (250 °F)
Fig. 6. Comparison of PV and YP of SAO andDrilling
WVO OBM. Fluid Systems
In the case of the low solids non-dispersed (LSND) mud
system, the ARC Eco-Lube showed lubricating performance
Fig. 6. Comparison of PV and YP of SAO and WVO OBM.
Fig. 6. Comparison of PV and YP of SAO and WVO OBM.
similar or better than diesel, SAO, and MOs, and thereby
20 demonstrates good lubricating potential, Fig. 9. The data
ft2)
20
15
ft2)
10 Sec Gel Strength 10 Min Gel Strength value with respect to the original COF value of the LSND
Gel Strength
15
10
mud. Comparison of the lubricating performance of the
Gel Strength
10
5 ARC Eco-Lube with respect to the CGL indicates better per-
5
0
formance for the CGL. This performance difference may be
SAO Mud (RT) SAO Mud SAO Mud WVO Mud (RT) WVO Mud WVO Mud
(120 °F) (250 °F) (120 °F) (250 °F) due to the presence of additional lubricating chemicals in the
0
Drilling
Mud Fluid Systems
SAO Mud (RT) SAO Mud
(120 °F)
SAO
(250 °F)
WVO Mud (RT) WVO Mud
(120 °F)
WVO Mud
(250 °F)
CGL. It may be mentioned that no additional materials were
Fig. 7. Comparison of 10 seconds and Drilling Fluid Systems
10 minutes gel strength of the SAO
Fig. 7. Comparison of 10 seconds and 10 minutes gel strength of the SAO and WVO OBM.
and added in the ARC Eco-Lube to enhance its lubricating poten-
WVO OBM.
tial. The data undoubtedly proves that the base stock devel-
Fig. 7. Comparison of 10 seconds and 10 minutes gel strength of the SAO and WVO OBM.
was formulated using the WVO-based base stock to assess its oped after esterification has significant potential to be used as
suitability to formulate an eco-friendly OBM system. Due to a green lubricant for oil and gas field applications.
the non-aqueous and eco-friendly nature of the base stock, it The second eco-friendly lubricant developed after treatment
will perform technically like a conventional OBM system and of the WVO using water + NaOH is known as the ARC
environmentally like a conventional WBM system, to explore Veg-Lube. Its performance was tested and evaluated in four
oil and gas resources without causing any detrimental impact different WBMs such as calcium chloride (CaCl2) mud, LSND
to other marine and terrestrial resources. mud, a potassium chloride (KCl) polymer mud, and bentonite
The PV and yield point (YP) data of the SAO and the mud, Fig. 10. Again, a CGL was also used for comparative
WVO OBM, Fig. 6, clearly indicates a much better rheologi- 0.40
0.40
cal property for the WVO OBM compared to the PV and YP 0.35
0.344
0.344
0.35
values of a conventional OBM system. Therefore, the newly 0.30
0.30
developed RWVO OBM will provide better cuttings carrying
0.25
0.25
capacity, and also hole cleaning efficiency compared to the
COF
COF
0.20
0.20
conventional OBM system. The analyses of the 10 seconds 0.158 0.158
0.15
0.15
and 10 minutes gel strength of the SAO and the WVO OBM, 0.126
0.126
0.10
0.10
Fig. 7, also indicate superior properties for the RWVO OBM
0.05
0.05
system. The higher gel strength of the mud will ensure ex-
0.00
0.00
cellent cuttings suspension capacity after the cession of the Bentonite Mud
Bentonite Mud
Bentonite + ARC Eco-Lube
Bentonite + ARC Eco-Lube
Bentonite + CGL
Bentonite + CGL
drilling operation. Measurement at room temperature, at 120 Bentonite Mud + Lubricant
Bentonite Mud + Lubricant
°F and also after thermal aging at 250 °F, indicates superior Fig. 8. The COF value of bentonite mud, bentonite mud + ARC Eco-Lube, and bentonite mud + CGL.
Fig.
Fig.8.8.The
TheCOF
COFvalue of bentonite
value mud, mud,
of bentonite bentonite mud + ARC
bentonite mudEco-Lube, and bentonite
+ ARC Eco-Lube, andmud + CGL.
properties for the RWVO OBM system compared to the con- bentonite mud + CGL.
ventional OBM system.
0.25
0.25 0.225
0.225
Green Lubricants Development 0.20
0.20 0.164
0.159 0.160 0.156
0.164
Two methods of chemical modification of the WVO, previ- 0.15 0.159 0.160 0.156
COFCOF
0.15
ously shown in Fig. 2, provided two base stocks as the end 0.105
0.10
0.105
products. Initially, the first base stock developed by esterifica- 0.10
tion of the WVO was tested using a standard lubricity tester 0.05
Invermul (ml) ®
12 0
0.21 0.2
0.17 ARC Eco-Mul (ml) 0 12
0.15
0.11 0.11 0.11
0.09 EZ-mul (ml) 4 4
0.05
Lime (g) 6 6
CaCl2 Mud LSND Mud KCl Polymer Mud Bentonite Mud Geltone (g) 4 4
Fig. 10. Comparative evaluation of the performance of WVO oil-based green lubricant — ARC Veg-Lube
Fig. Duratone (g) 6 6
in the 10. Comparative
presence evaluation
of various WBM systems. of the performance of WVO oil-based green
lubricant — ARC Veg-Lube in the presence of various WBM systems. Brine (61 g CaCl2
85 85
in 85 cc water) (ml)
assessment of the performance of the newly developed green
Barite (g) 161 161
lubricant ARC Veg-Lube. The dataFormulation
Formulation clearly shows that even
Mud System
Invermul ®
ARC Eco-Mul
at a 1%
SAO (ml) concentration, the
218 newly developed
218 green lubricant Table 1. Invert emulsion mud formulation using Invermul® and ARC Eco-Mul
Invermul (ml)
®
12 0
was able
ARC Eco-Mul (ml)to significantly knock
0 down the
12 COF values of all
EZ-mul (ml)
the
Lime mud
(g) systems. This observation
4
6
4
is reflected
6 by a 46% re- °F. Therefore, the results demonstrate the suitability of the
Geltone (g) 4 4
Duratone (g)in the COF value6 of the CaCl26 mud, 45% reduction
duction WVO-based emulsifier for designing OBM systems with ES
Brine (61 g CaCl in 85 cc
of
2
the(ml)COF value of the 85
water) LSND mud, 86% 85 reduction of the values that are sufficient to create a tight emulsion in the mud
Barite (g) 161 161
COF value of the KCl polymer mud, and an 82% reduction system.
®
Table 1. Invert emulsion mud formulation using Invermul and ARC Eco-Mul
of the COF value of the bentonite mud. With respect to the Figure 12 shows the HPHT spurt and fluid loss behavior of
3% CGL containing mud, the 1% ARC Veg-Lube containing the new and commercial emulsifier containing muds measured
mud showed a lower performance in the CaCl2 mud, a similar at 300 °F and 500 psi. The data clearly indicates the superior
performance in the LSND mud, and a better performance in fluid loss behavior of the ARC Eco-Mul containing mud sys-
the KCl polymer and bentonite mud. tem compared to the mud containing the commercial primary
emulsifier. Due to the ability of the emulsifier to create a tight-
Eco-Friendly Emulsifier er and stable emulsion, there was no spurt loss in the mud
containing the newly developed primary emulsifier. The tight-
An eco-friendly emulsifier known as ARC Eco-Mul was syn- ness350of the emulsion is further reflectedOBMby+ ARC
OBM + Commercial Emulsifier
a very
Eco-Mul
low all oil
300
thesized by chemical modification of WVO by treating it with 350
250
ES ValueES Value
8
Figure 11 shows the ES values of the OBM + commercial Spurt Loss Fluid Loss
primary emulsifier containing mud, along with the ES values 4 3.4
6 5.6
of the OBM + ARC Eco-Mul. The results indicate good ES
2
values for both of the mud systems. A comparative assess-
4 3.4
ment of the ES values of the two mud systems shows higher 0.4
0
0
ES values for the OBM containing commercial emulsifier. 2
Invermul ARC Eco-Mul
OBM Systems
Both of them created a tight emulsion in the invert emulsion
0.4
mud systems. This was reflected by having no separation Fig.12.
Fig. 12.The
The HPHT
HPHT spurtspurt andloss
and fluid fluid lossInvermul
of the of the ®Invermul 0 and ARC
and ARC®Eco-Mul Eco-Mul
formulation (tested at 300 °F
and a 0pressure of 500 psi).
formulation (tested at Invermul
300 °F and a pressure of 500 psi).ARC Eco-Mul
of the phases, both before and after the hot rolling at 300 OBM Systems
6 SPRING 2019 SAUDI ARAMCO JOURNAL OF TECHNOLOGY Fig. 12. The HPHT spurt and fluid loss of the Invermul® and ARC Eco-Mul formulation (tested at 300 °F
and a pressure of 500 psi).
Mud System
O/W Ratio 80/20 80/20 80/20 80/20
SAO (cc) 218 218 218 218
ARC Eco-Mul (cc) 12 6 4 0
EZ-Mul (cc) 4 4 4 4
Lime (g) 6 6 6 6
Geltone (g) 4 4 4 4
Duratone (g) 6 6 6 6
Brine (61 g CaCl2 in 56.6 cc water 85 85 85 85
Barite (g) 161 161 161 161
Table 2. Screening of the concentration of ARC Eco-Mul to identify the optimum range
8
6
Spurt Loss Fluid Loss
range of the ARC Eco-Mul, Table 2. API and HPHT fluid
Filtrate
8
Figure 14 shows the HPHT spurt loss measured at 300 °F
Filtrate
8 6
6
and 500 psi using various concentrations of ARC Eco-Mul.
Filtrate
6
6
4 The data clearly indicates some spurt loss at a concentration
4 2
of 6 cc/350 cc lab mud, and a higher spurt loss with a reduced
2
2
concentration. The OBM with an ARC Eco-Mul concentra-
2
0
0
tion of 12 ppb shows virtually no spurt loss. Based on this
12 6 4 0
0
0
ARC Eco-Mul Concentration (cc/Lab bbl)
information, it can be concluded that a concentration range
12 6 4 0
ARC Eco-Mul Concentration (cc/Lab bbl) of 8 cc to 12 cc for 350 cc of lab mud will provide desirable
Fig. 14. The HPHT spurt loss for formulations having different concentrations of ARC Eco-Mul (tested at
300 °F and a pressure of 500 psi). HPHT fluid loss behavior.
Fig. 14.
Fig. 14.The
TheHPHT
HPHTspurt spurt
loss forloss
formulations having different
for formulations concentrations
having different of ARC Eco-Mul (tested
concentrations ofat
300 °F and a pressure of 500 psi).
ARC Eco-Mul (tested at 300 °F and a pressure of 500 psi).
Figure 15 shows the HPHT fluid loss measured at 300 °F
and 500 psi using various concentrations of ARC Eco-Mul.
80 The data clearly indicates acceptable HPHT fluid loss behav-
70 68
ior at a concentration of 6 ppb and higher. The OBM with
60 a 12 cc ARC Eco-Mul concentration shows only 3.4 cc fluid
loss. The data again indicates that a concentration range of 8
Filtrate (ml)
50
10 7
3.4
Eco-Friendly Spotting Fluid
0
12 6 4 0
ARC Eco-Mul Concentration (cc/Lab bbl)
Pipe sticking while drilling is one of the major drilling chal-
Fig. 15.
Fig. 15. The
TheHPHT
HPHTfluid loss
fluidforloss
300 °F and a pressure of 500 psi).
formulations having different
for formulations concentrations
having different of ARC Eco-Mul (tested
concentrations ofat lenges that we face in most of our drilling operations. Some
ARC Eco-Mul (tested at 300 °F and a pressure of 500 psi).
of the critical factors that can trigger a pipe sticking event are
50
SAUDI ARAMCO JOURNAL OF TECHNOLOGY SPRING 2019 7
40 38.24
improper drilling practices, inadequate hole cleaning, wellbore mud in the absence of any spotting fluid, to use as base line
instability, excessive reaming or back reaming, poor mud information. Table 3 lists the various spotting fluids used to
rheology, deposition of thick mud cake, the presence of a high evaluate their ability to reduce the SBM and the USBS. The
permeable formation, quality of the mud, and the deposited mud cake was prepared by running a filtration test for more
mud cakes, etc.12-15. than 48 hours at 100 psi and at an ambient temperature7. The
Various types of aqueous and non-aqueous spotting fluids tests were conducted after 6 and 16 hours of soaking time,
are used by the industry to recover a stuck pipe. Conventional using mud cake of a similar thickness, and deposited by the
non-aqueous spotting fluids are commonly designed using same drilling mud, i.e., weighted KCl polymer mud. Figures
diesel, MOs, or base stocks derived from these oils. Due to 16 to 19 show the SBM and the USBS of the base mud cake,
negative environmental characteristics, poor biodegradation and also the mud cakes tested after 6 and 16 hours of soaking
properties and unacceptable toxicity, these oils have severe time in the presence of various spotting fluids, respectively.
restrictions for sensitive environments. Therefore, the industry Figure 16 shows the average SBM of the original mud cake
needs an eco-friendly base stock to formulate green spot- and also the mud cakes soaked for 6 hours in various spotting
ting fluids to overcome the limitations of non-eco-friendly fluids. A comparison of average SBMs of the original mud
spotting fluids used by the industry. Bearing this in mind, an cake and the various spotting fluid soaked mud cakes indicate
eco-friendly base stock derived from WVO has been used to that all the spotting fluids reduce the SBM of the mud cake
formulate a green spotting fluid known as ARC Eco-Spot. Ta- as a result of weakening, damage, and degradation of the
ble 3 shows the formulation of the ARC Eco-Spot along with sticking bonds, due to the interactions of the spotting fluids
three conventional spotting fluids to compare and evaluate the with the mud cakes at the mud cake spherical foot interface.
performance of the newly developed ARC Eco-Spot. The data further shows that the glycol-based spotting fluid,
To evaluate the performance of the ARC Eco-Spot, tests fluid C, shows the maximum reduction in SBM, the non-en-
were conducted to determine the sticking bond modulus vironment friendly spotting fluid, fluid B, caused the second
(SBM), and ultimate sticking bond strength (USBS) of a 10 maximum reduction in the SBM after 6 hours of soaking time,
mm thick mud cake, deposited by a weighted KCl polymer and spotting fluid A shows the minimum reduction in SBM.
Spotting Fluid A
Components Field Formulation (bbl) Concentration (%) Lab Formulation (cc)
Diesel 64 0.64 224
E-Z Spot 8 0.08 28
Water 28 0.28 98
Total Volume 100 350
Spotting Fluid B
Components Field Formulation (bbl) Concentration (%) Lab Formulation (cc)
Diesel 64 0.64 224
Pipe-Lax 8 0.08 28
Water 28 0.28 98
Total Volume 100 350
Spotting Fluid C
Components Field Formulation (bbl) Concentration (%) Lab Formulation (cc)
Glycol 85 0.80 281
Lubricant 16 0.15 52
Pipe-Lax 5 0.05 17
Total Volume 106 350
ARC Eco-Spot
Components Field Formulation (bbl) Concentration (%) Lab Formulation (cc)
Eco-Friendly Base Fluid (cc) 64 0.64 224
E-Z Spot (cc) 8 0.08 28
Water (cc) 28 0.28 98
Total Volume 100 350
Filtrate (ml)
50
performance is comparable to the performance of the com-
40
mercial spotting fluid B. The data clearly indicates that the
newly developed ARC Eco-Spot has either a similar or better 30
(kgf/mm)
33.92
SBM(kgf/mm)
a longer soaking time for effective damage and degradation of 40 38.24 30.43
30
the mud cake. 30
SBM (kgf/mm)
25.8826.361
SBM
30.43
22.68 23.08
Interestingly, spotting fluid B indicates an increase in SBM 30
22.28 21.65
26.361
20
20
value after 16 hours of soaking time compared to the SBM 22.28 23.08
20
value determined after 6 hours of soaking time. This indicates 10
10
that spotting fluid B has a time dependent stiffening effect, 10
and therefore, causes an increase in SBM. This indicates that 00
Base
Base Mud
Mud Cake
Cake Spotting
SpottingFluid-A
Fluid-ASpotting Fluid-B
Spotting Spotting
Fluid-B Fluid-C
Spotting ARCARC
Fluid-C Eco-Spot
Eco-Spot
for some spotting fluids, soaking beyond an optimum time 0
Mud Cake + Spotting Fluid
Base Mud Cake Spotting Fluid-AMud Cake +Fluid-B
Spotting Spotting Fluid Fluid-C ARC Eco-Spot
Spotting
period may make it more difficult to recover a stuck pipe. Fig. 16. Experimentally determined SBM ofMud Cake +and
the original Spotting
variousFluid
spotting fluid soaked mud cakes, after
Fig.
6 17. Experimentally
hours soaking time.determined SBM of the original and various spotting fluid soaked mud cakes, after
Subsequently, identification of the optimum soaking time of Fig.
16 17.ofofExperimentally
hours soaking time. determined SBM of the original and various spotting fluid
Fig. 17. Experimentally determined SBM of the original and various spotting fluid soaked mud cakes, after
soaked
16 hours mud cakes,
time.after 16 hours of soaking time.
various spotting fluids is very important to recover a stuck of soaking
8
pipe easily and quickly. The newly developed ARC Eco-Spot
8
showed no or negligible time dependent stiffening effect, and
6.01
therefore has a superior long-term behavior compared to spot- 6 6.01
(kgf)
6
ting fluid B. This fluid causes degradation and weakening of
(kgf)
USBS
4
4
and therefore has a superior short-term behavior compared to 2.81
2.81
spotting fluid A. Recovery of a stuck pipe after a short soak- 2
2 1.45
ing time has high technical and economic benefits. 1.27
1.27
1.45
0.6
Figure 18 shows the average USBS of the original mud cake 0.6
0
and also the mud cakes soaked for 6 hours in various spotting 0
Base Mud Cake Spotting Fluid-A Spotting Fluid-B Spotting Fluid-C ARC Eco-Spot
Base Mud Cake Spotting Fluid-A Spotting Fluid-B Spotting Fluid-C ARC Eco-Spot
fluids. The comparison of the average USBS of the original MudCake
Mud Cake++Spotting
SpottingFluid
Fluid
mud cake and the mud cake soaked for 6 hours indicate that Fig.
Fig. 18.
18. Experimentally determined USBM
Experimentally determined USBMof
ofthe
theoriginal
originaland
andvarious
variousspotting
spottingfluid
fluidsoaked
soaked mud
mud cakes,
cakes,
after
after 66
Fig. hours
18. of
of soaking
Experimentally
hours time. determined USBM of the original and various spotting
soaking time.
all of the spotting fluids reduced the USBS of the mud cake
fluid soaked mud cakes, after 6 hours of soaking time.
as a result of weakening, damage, and degradation of the
sticking bonds, due to the interactions of the spotting fluids 8
with the mud cake. The data further shows that spotting fluid 6.01
6
C caused the maximum reduction in USBS after 6 hours of
USBM (kgf)
Dr. Tao Chen, Dr. Qiwei Wang, Dr. Fakuen F. Chang, and Amro E. Mukhles
Table 2. The typical formation water chemistries, gas analysis (%), gas-water
where a = g × C. Here, a1 and a2 are the activity of scaling production rates, and the reservoir pressure and temperature applied in scale
prediction
cation and anion in the solution, respectively. K is normally
4
Fe + 2 HCl → FeCl2 + H2 (2)
3
2
The test coupon was immersed in corrosion inhibited 26
wt% HCl acid over half an hour at 125 °C. The surface area 1
Fig. 1. The pH of mixing spent acid and formation water saturated with sour gases.
25000
Table 3. Weight change of the T-95 coupons before and after field application
600 20000
conditions previously shown in Table 2. The coupon was
400
15000 retrieved after 3 months for post-analysis.
10000 Table 3 shows the overall weight change of the T-95
Iron sulfide (mg/L)
200
5000
coupons before and after field application. The weight change
Iron sulfide (SR)
is composed of the weight loss due to corrosion — reducing
0 0
0 10 20 30 40 50 60 70 80 90 100 weight — and the weight gain due to the formation of scale
% Spent Acid
on the coupon surface — increasing weight. A minor weight
Fig. 2. Iron sulfide scale prediction when spent acid mixes with formation water
Fig. 2. Iron sulfide scale prediction when spent acid mixes with formation water saturated with sour increase of 0.049 g was measured for the T-95 coupon after
gases
under reservoir conditions.
saturated with sour gases under reservoir conditions. field application.
Figure 3a is a photograph of the T-95 carbon steel coupon
with sour gases under reservoir conditions.
before field application, and Fig. 3b is a photograph of the
The pH of 100% spent acid saturated with sour gases is
same coupon and after being retrieved from 3 months of
3.75. When it mixes with formation water saturated with sour
exposure in the field. Before field application, the coupon
gases, the pH increases. At the ratio of 10:90 mixing of spent
surface was mechanically polished without any deposition
acid and formation water saturated with sour gases, the pH
or corrosion. Weight A thin Before Weight
layer (g)
of black Before Weight
(g) After
deposition wasWeight(g)
observed After
Weight
(g) Chang W
increases to ~5.94. The pH increases with a further increase T-95 Coupon in T-95 Coupon 117.821 117.821 117.880 117.880 0.049
on the surface of the test T-95 coupon after field application.
the ratio of formation water until it reaches a pH of 6.82 in
Based on visual observation, there was a certain amount of
100% formation water. A higher pH favors precipitation of
Table 3. Weight Table change
corrosion3. Weightof thechange
byproduct T-95orcoupons
of thedeposited
scale T-95
before couponsandthe
on after
before
surfacefieldand application
of after field applicat
the
certain scales, e.g., calcium carbonate, iron sulfide, and iron
coupon during the 3 months of field application.
carbonate.
Figure 4 is the optical image of the surface of the T-95 car-
Iron sulfide scale was predicted to form when spent acid
bon steel coupon; before field application, Fig. 4a, and retrieved
mixes with formation water saturated with sour gases under Weight Before
after from Weight Before (g) (g) Weight Weight
After After
(g) (g)Fig.WeightWeight
Change Change (g)
No (g)
reservoir conditions, Fig. 2. T-95 T-95
CouponCoupon3 months of exposure
117.821
117.821
in the
117.880
field,
117.880 4b.
0.0490.049
Fig. 6. The EDS cross-section of the T-95 coupon after field application.
against further corrosion for long periods of time6, 13.
Fig. 6. The EDS cross-section of the T-95 coupon after field application.
Over the past decade, great efforts have been made to
pyrrhotite
7000
• Pyrrhotite
pyrrhotite
• Pyrite
6000
• Marcasite
pyrrhotite
• Iron
pyrite
5000
Counts
pyrite
4000
pyrite
pyrite
pyrite
pyrite
3000
marcasite
2000
1000
0
10 20 30 40 50 60 70 80
Modiu L. Sanni, Frode Hveding, Dr. Sunil L. Kokal, and Ibrahim M. El-Zefzafy
ABSTRACT INTRODUCTION
Fiber optic sensing technology has gradually become one of Innovative wellbore monitoring using fiber optic distributed
the pervasive tools in the monitoring and surveillance toolkit acoustic sensing (DAS) and distributed temperature sensing
for reservoir and production engineers. Traditionally, sensing (DTS) improves the information available for reliable deci-
with fiber optic technology in the form of distributed acous- sion making for effective reservoir management. Downhole
tic sensing (DAS) or distributed temperature sensing (DTS), data acquisition by fiber optic sensing enables the user to
and most recently, distributed strain sensing and distributed obtain information across the entire reservoir simultaneously.
chemical sensing, were done with the fiber being perma- Another level of information beyond the traditional wireline
nently clamped either behind the casing or production tubing. conveyed production logging tool (PLT) techniques is cap-
Clamping the fiber behind the tubing or casing is sometimes tured because of the nature of fiber optic sensing. The user
beleaguered with operational challenges that often lead to ren- can observe in real-time the dynamic environment across the
dering the fiber partially damaged or inoperable. The emer- entire sensing area during production or injection changes and
gence of the composite carbon rod system that can be easily can act accordingly.
deployed in and out of a well, similar to wireline logging, has There are three main methods for getting fiber optics down
made it possible to sense any well without prior fiber optic into the wellbore, exposed to the variations in temperature
installation. and noise, i.e., production or injection1. These methods are
In this article, we present the lessons learned from the first permanent installations, semi-permanent installations and
well where we deployed in-well fiber optic DAS/DTS. The use intervention-based service.
of DAS/DTS was done in a few vertical oil producer wells Permanent installation is obtained by strapping a fiber optic
and water injector wells without prior fiber optic installation. line outside the casing and cementing it in place, Fig. 1a. Fiber
The key objectives of the tests were to: (1) investigate the can then be used to observe the heat being generated during
well integrity across the entire length of each well, (2) assess curing and so give indications of the height of cement, and also
the production and injection flow profile across the perfora- the potential quality. In addition, since the fiber is directly cou-
tions and behind casing, which to now, was not possible with pled to the sandface, it will be able to provide good information
a conventional production logging tool (PLT), and (3) inves-
tigate the possibility of using the combination of a distrib-
uted acoustic survey and a distributed temperature survey for
quantitative production flow analysis.
This article reviews the complete design and implementa-
tion of the in-well fiber optic deployment, field operational
issues, analyses, and interpretation of the sensing results.
The combination of DAS/DTS data showed no well integrity
related issues. The sensing data surprisingly pinpointed a few
geological features such as cooling shallow aquifers that until
now had not been noticed. The combination of different pulse
widths during shut-in and the production and injection cycles
helped to refine the resolution of the flow profile from the (a) (b) (c)
production and injection zones.
Sensing Program
Flow Allocation
Flow Allocation PW 20 ns
Repeat PW 50 ns
Open Open Open Closed Open Closed Open Open
Production-1b 50
Production-1a 20
Production-2 20
Production-3 50
End of Sensing
Shut-in 1 20 ns
Shut-in 2 50 ns
Record DTS on
Record DTS on
Beginning of
POOH while
Producing
Producing
the Spool
RIH while
the Spool
Sensing
ns PW
ns PW
ns PW
ns PW
PW
PW
24
15 min 4 hours 2 + 2 hours 2 hours 4 hours 2 hours 4 hours 15 min
hours
Total: 44.5 hours
Depth (ft)
liner and tubing to a depth of x465 ft. The perforated interval
spans from x070 ft to x105 ft. The rig-up process involved
rigging up the flanged wellhead crossover and blowout pre-
venter (BOP). The modular Quad BOP (top, blind, slip, pipe)
was function tested. Then the dual stripper, lubricator, and
gooseneck were rigged up on the injector. The carbon rod was
then stabbed into the injector and the gooseneck rollers were
closed. The injector and stripper were rigged up on the BOP.
Thereafter, the BOP rams, the strippers, and the lubricator Fig.
Fig. 5. RIHdata
5. RIH data—— weight
weight andand depth
depth vs. time.
vs. time.
Weight (lb)
WHP (psi)
were pressure tested to 2,500 psi. The run in hole (RIH) pro-
cess began after a safety meeting was held to review all the
details of the sensing operations.
The well was opened fully while the carbon rod was at 610
Weight (lb)
ft as per the sensing program. A set down weight of -2,000 lb
WHP (psi)
was noticed when the carbon rod was at x192 ft. The weight
drop was due to the well’s high flow rate. It was then decided
to shut-in the well while RIH. Pull tests were performed at
Fig. 6. Carbon rod weight and well flow vs. time for production-1 sequence.
every 1,000 ft or when needed to confirm the rod weight, and
that nothing was holding the rod, Fig. 5.
After reaching the desired total depth (TD) at x262 ft, it
was decided to start the sensing operation as per the program
Fig. 6. Carbon rod weight and well flow vs. time for production-1 sequence.
Fig. 6. Carbon rod weight and well flow vs. time for production-1 sequence.
— production-1a. The well was gradually opened from 10%,
25%, 45%, 65%, 75%, to 100% fully open. It was observed
that the weight of the carbon rod dropped as the choke was
opened more, Fig. 6.
Figure 7 shows the carbon rod weight and well flow vs.
Weight (lb)
WHP (psi)
Weight (lb)
WHP (psi)
Fig. 11. DAS overview plot of the entire sensing sequence from the top to the TD.
Fig. 11. DAS overview plot of the entire sensing sequence from the top to the TD.
RESULTS AND DISCUSSIONS Date and Time
convection. The DAS and DTS images, Fig. 12, only show evi-
dence of convection inside the wellbore at the aquifers because
From11.
Fig. the DAS
data analyses,
overview there wasofnothe
plot strong evidence
entire of thefrom
of sequence
sensing high the
temperature contrast.
top to the TD.
any well integrity issues or leakage at the aquifers. The Quantitative analyses of the production flow profile was
shut-in temperature peaks previously shown in Figs. 9 and done using the sensing data from the DAS/DTS survey, pres-
11, develop parallel to one another vs. depth, with no sign sure, reservoir description and deviation data as inputs into
of upward or downward fluid movement other than gravity the flow simulation model to quantify the production from
Fig. 12. DTS water fall vs. DAS (derivatives) along the entire wellbore.
the different zones. The data acquired from the different PWs flow rate was not anticipated during the planning stage.
during shut-in and production cycles helped to refine the ver- Apparently, the carbon rod has never been used in any well
tical resolution of the flow profile from the production zones. with a flow rate exceeding 5,000 bpd. Although the carbon
A shorter PW is generally a tradeoff between resolution and rod is very strong — over 22,000 lb tensile capacity — and
energy response, and it could be challenging to obtain suffi- quite different from the CT, its compressive strength — less
cient signal-to-noise ratio with a shorter PW. Since the pro- than 2,200 lb — limits its application in very high rate
duction rate for the well was very high, the odds were favor- wells without additional weight attached to the BHA.
able, Fig. 13.
2. Consequently, a best practice for logging high rate wells
Figure 14 shows the quantitative flow rate and flow profile
results from the integration of the independent DAS and DTS is to simulate helical buckling and establish the maximum
data. It is worth noting that using the DTS data alone can safe production flow rate for each well’s flowing condition
generally lead to a non-unique production inflow profile. It is prior to logging.
usually a best practice to constrain the model with the DAS 3. Where possible, and if it will not adversely affect the
data and better vertical resolution with varying PWs. The data sensing program, consider keeping the well at shut-in
showed thatProduction-1b,
the lower zone isPWthe main contributor
= 50(derivatives)
ns (10 m) of the Production-1a,
during RIH PW
and = 20 nsoperations
POOH (4 m) to prevent helical
Fig. 12. DTS water fall vs. DAS along the entire wellbore.
water inflow while theBandbulk 20 ~100
of the gasHz
and oil is apparently Band and/or
buckling 20 ~100 Hz axial force.
excessive
coming from the top zones.
4. For technology trials, it is always good to consider a gamut
of “what ifs” and anticipate different scenarios that may
Fig.
KEY 13. DAS image
LESSONS LEARNED PW vs. resolution across the production intervals.
become a potential show stopper.
1. Helical buckling of the carbon rod due to a very high 5. A post-job detailed examination of the cracked carbon rod
Fig. 13. DAS image PW vs. resolution across the production intervals.
Fig. 13. DAS image PW vs. resolution across the production intervals.
SAUDI ARAMCO JOURNAL OF TECHNOLOGY SPRING 2019 27
Fig. 14. Quantitative analyses of the flow rate and flow profile results.
Fig. 14. Quantitative analyses of the flow rate and flow profile results.
showed no evidence of chemical damage or any reduction lower zone is the main contributor of the water inflow,
in physical properties as compared to the reference while the bulk of the gas and oil is apparently coming from
(original) samples. the top zones.
CONCLUSIONS ACKNOWLEDGMENTS
1. The first field trial of the carbon rod in our operations The authors would like to thank the management of Saudi
showed it has great potential. The field trial was paused Aramco for their support and permission to publish this arti-
because of the crack on the carbon rod. A post-job review cle. This article would not have been possible without the
showed that the crack developed due to helical buckling of contributions and efforts of many colleagues. In particular we
the rod as a result of a high flow rate that the carbon rod would like to acknowledge and thank Nabil Bulushi, Abdul-
encountered while RIH. A simulation of the well’s flowing lah Ghamdi (Lafi), Ahmed Alsmaeil, Saad Al-Otaibi, Tariq
condition and carbon rod showed that severe helical Buzaid, Alex Crossland, Neil Gardner, and many others for
buckling caused compression crumpling of the carbon rod their contributions toward the project.
once the flow rate exceeded a maximum safe production This article was presented at the SPE Annual Technical
flow rate. Conference and Exhibition, Dallas, Texas, September 24-26,
2018.
2. The data obtained showed no well integrity issues across
the entire length of the well. Using the DTS data alone
REFERENCES
would have raised a false alarm about well leakage around
the shallow aquifers. The combination of the DAS and
1. Al Shoaibi, S., Kechichian, J., Mjeni, R., Al Rajhi, S., et
DTS data only show evidence of convection inside the
al.: “Implementing Fiber Optics Distributed Sensing as a
wellbore at the aquifers because of the high temperature
Key Surveillance Tool,” SPE paper 183535, presented at
contrast.
the Abu Dhabi International Petroleum Exhibition and
3. The sensing data surprisingly revealed the possibility of Conference, Abu Dhabi, UAE, November 7-10, 2016.
detecting active shallow aquifers. This is not possible with
2. Danardatu, H., Gregersen, S.H.H., Alterrn, E. and
conventional PLT.
Pellegrini, I.: “Data Acquisition and Processing of Carbon
4. The data obtained was used for quantitative analyses of Rod Conveyed DTS and DAS in Very Long Horizontal
the production flow profile. The data acquired from the Wells. First Trial in North Sea Danish Sector,” SPE paper
different PWs during the shut-in and production cycles 170663, presented at the SPE Annual Technical Conference
helped to refine the vertical resolution of the flow profile and Exhibition, Amsterdam, the Netherlands, October
from the production zones. The analysis showed that the 27-29, 2014.
formulations.
Aliquots of crushed core and residual solids from the xylene
treated sludge samples were assessed for their mineralogical
EXPERIMENTAL STUDY
composition by using the X-ray diffraction (XRD) technique,
Table 2.
Materials
Additive Concentration
Freshwater/NH4Cl 4 to 6 wt%
Mutual solvent 10 vol%
Surfactant 0.2 to 0.3 vol%
HCl acid 10 wt%
Formic acid 5 wt%
Acetic acid, iron reducing
10 gal/1,000 gal
agent
Citric acid, iron chelating
50 lb/100 gal Fig. 1. A bituminous sediment sample (sludge type 1) from an organic rich layer
agent
in a sandstone reservoir. The samples have a black vitreous luster with conchoidal
Corrosion inhibitor 5 gal/1,000 gal fractures. They represent the filling of available porosity because of the thermal
conversion of kerogen. Their microscopic appearance reflects the shape of the void
Fig. 1. A bituminous sediment sample (sludge type 1
Table 1. Typical acid recipe used in compatibility and coreflood testing they fill.
Fig. 2. Type 2 sludge samples, a soft and oily material in fine- to medium-grained matrix.
Fig. 2. Type 2 sludge samples, a soft and oily material in fine- to medium-grained matrix.
Mineral Concentration (wt%)
Quartz (SiO2) 73 80
Plagioclase (CaAl2Si2O8 or NaAlSi3O8) 2 1
Orthoclase (KAlSi3O8) 2 1
Mineral
Siderite (FeCO3) Concentration (wt%) 9 6
Quartz
Smectite (SiO 2) 73 804 3
Plagioclase (CaAl2Si2O8 or NaAlSi3O8) 2 1
Illite (K, H3O) (Al, Mg, Fe)2(Si, Al) 3 2
Orthoclase (KAlSi3O8) 2 1
Kaolinite (Al
Siderite (FeCOSi O (OH)4)
2 2 5 3) 9 66 5
Smectite
Table 4
2. Generalized mineralogical analysis conducted by XRD of the sandstone samples 3
Illite (K, H3O) (Al, Mg, Fe)2(Si, Al) 3 2
Kaolinite (Al2Si2O5(OH)4)
Pyrolysis 6 Solubility 5
Testing
Selected
Table 2. sludge samples were
Generalized analyzed usinganalysis
mineralogical a high resolu-
conductedThe
bysolubility
XRD ofofthe
thesandstone
type 2 sludge samples
samples was examined in
tion pyrolysis method — the HAWK Petroleum Assessment various acids and solvents. The samples were soaked in the
Method (PAM)TM by Wildcat Technologies. An aliquot of 40 fluid mixtures at 160 °F for 16 to 20 hours in an oven. The
mg of powdered rock or oil mixed with clean sand is put in a solubility values were calculated based on the sample’s dry
crucible and then inserted in a pyrolysis oven. In a single run, weight before and after solubility testing. The fluid samples
the oven heats the sample in an inert condition at five isother- were filtered using 0.45 µm filter paper following the solubil-
mals separated by multiple ramps of 25 °C per minute. This ity experiments. The sludge samples were dried at 212 °F for
generates five peaks in a pyrogram — the pyrolytic response 16 to 20 hours prior to the weight measurements.
of the sample — assigned to specific hydrocarbon ranges.
Coreflood Experiments
Organic Microscopy
The coreflood system was used to measure the pressure drop
Selected bituminous sediment samples were studied using across the core plugs. Potassium chloride (KCl) brine was
organic petrology. Whole rock plugs were prepared using injected at the beginning at flow rates of 1.0 cm3 per minute,
a cold setting epoxy resin. These were polished and detrital 2.0 cm3 per minute, and 3.0 cm3 per minute to measure differ-
organic matter fragments were identified microscopically in ential pressure and test the quality. The acid recipe was then
reflected and fluorescent light. The standard technique of coal injected into the core plug, followed by the brine fluid. The
petrography4 and the reflectance investigation technique5 were experiments were conducted at 160 °F, 1,000 psi pore pres-
used. The preparation method of whole rock plugs are best sure, and 2,000 psi confining pressure.
described by Sachse et al. (2012)6.
Fig. 3. Bituminous sediment samples include a mixture of coal and kerogen particles. Scale bar = 100 μm.
Fig. 3. Bituminous sediment samples include a mixture of coal and kerogen particles. Scale bar = 100 µm.
Fig. 4. Two phases of solid bitumen: A dominant phase with moderately strong, orange-brown fluorescence, and a subordinate phase with strong, green-yellow
Fig. 4. Two
fluorescence. phases
The moderately of green-yellow
strong solid bitumen:
fluorescence A dominant
of mounting phase
epoxy (me) withof moderately
is the result strong,
epoxy acting as an organic orange-brown
solvent and extracting oil out of bitumen
fluorescence, andlight,
(a, b, and c). Reflected white a subordinate
oil immersion; (d, e,phase
and f) bluewith strong,oil green-yellow
light irradiation, immersion. Scale bar =fluorescence.
100 μm. The moderately strong
green-yellow fluorescence of mounting epoxy (me) is the result of epoxy acting as an organic solvent and
RESULTS AND
extracting oil DISCUSSION
out of bitumen (a, b, and c). Reflected white geochemical
light,techniques.
oil immersion;Such materials
(d, e, can
andbef)found
blueduring
light
irradiation, oil immersion. Scale bar = 100 µm. operations in siliciclastic reservoirs. The bituminous sediment
Fig.
Sludge 4. Two phases of solid bitumen: A dominant phase
Characterization witharemoderately
samples fine-grained and strong, orange-brown
gray, and include relatively big
fluorescence, and a subordinate phase with strong, green-yellow fluorescence. The moderately strong
particles of solid bitumen with black color, vitreous luster,
green-yellow fluorescence of mounting epoxy (me) isand theconchoidal
result offractures.
epoxy acting as an organic solvent and
They are also characterized by a
Bituminous sediments — type 1 sludge — were characterized
extracting oil out of bitumen (a, b, and c). Reflected white light, oil immersion; (d, e, and f) blue light
for their composition with variable organic microscopic and strong odor of diesel or synthetic oil. The pyrolysis analysis
irradiation, oil immersion. Scale bar = 100 µm.
34 SPRING 2019 SAUDI ARAMCO JOURNAL OF TECHNOLOGY
suggests that the samples contain solid bitumen contaminated
100 Original Sample
Original
with diesel or synthetic oil. They most probably represent the
100
100 Original Sample
Sample
80 filling of available porosity because of the thermal conversion
(mV)
80
80 of kerogen and or severe biodegradation of the reservoir oil.
(mV)
(mV)
60 The organic microscopic assessment indicates that the sam-
60
FID
60
40
ples contain a mixture of coal fragments, and solid bitumen
FID
FID
40
40 embedded in the mineral groundmass. The coal fragments
20 contain diverse kerogen types, which include vitrinite, cutinite,
20
20 resinite, sporonite, and exsudatinite, Fig. 3. Occasionally, the
0
(a) 00 0 200 400 600 800 vitrinite is surrounding the resinite, which does not appear to
0
0 200
200 400
Time
400 (min) 600
600 800
800 be fluorescence. This difference in fluorescence properties is
Time
Time (min)
(min) commonly used to distinguish macerales from each other.
The presence of a darker rim around the outside of the
100 Sample after solvent extraction
100 Sample
Sample after
after solvent
solvent extraction
extraction
maceral, Figs. 3a and 3 , is also a common feature that is
100
80 sometimes called a reaction rim caused by weathering of the
80
(mV)
40
40 green-yellow fluorescence, Fig. 4.
20
20 In further investigation of the hydrocarbon type, a sample
20
(b) 0 was analyzed by using the high resolution pyrolysis method
0
0 0 200 400 600 800
— PAM™, Fig. 5. The sample was analyzed before (bulk) and
0
0 200
200 400 600 800
Time
400 (min) 600 800
after the methanol, acetone, and chloroform extraction, Figs.
Time
Time (min)
(min) 5a and 5b. A 3.6% diesel solution mixed with clean sand
50 was run by the same methods, Fig. 5c. The sample before
50
50 3.65 Diesel extraction shows peaks indicating a light, and a very heavy
40 3.65
3.65 Diesel
Diesel hydrocarbon mixture. The PAM pyrogram of the extracted
40
(mV)
30
(mV)
30
solid hydrocarbon. The combination of the diesel and the
30
FID
20
20 shown that Fig. 5d looks identical to the pyrogram of the
10 original sample in Fig. 5a. Therefore, it can be concluded that
10
10
(c) this sample contains indigenous solid bitumen mixed with die-
0
0
sel or synthetic oil from drilling fluids.
0 0 200 400 600 800
0
0 200
200 Time
400(min)
400 600
600 800
800 A part of the sample was treated with xylene to remove all
Time
Time (min)
(min) types of hydrocarbons, and then these were characterized by
450 XRD analysis for their mineral composition. The solubility
400 test indicates that the 70 wt% of the sample is solid bitumen
350 Sample after extraction
and 30 wt% is sediment. The XRD analysis revealed that the
300 3.65 Diesel
inorganic component of the sample is composed of calcite (82
FID (mV)
250
wt%), quartz (16 wt%), microcline feldspar (1 wt%), and
200
halite (1 wt%), Table 3. The absence of clay eliminates the
150
100
potential for swelling, and any pore problems.
50 The fact that the sample is almost completely dissolved
(d) 0 in xylene confirms that this sample is a solid bitumen rather
0 200 400 600 800
Time (min) Compound Concentration (wt%)
Calcite (CaCO3) 82
Fig. 5. Pyrolytical results of the bituminous sediment sample using the PAMTM: Quartz (SiO2)TM 16
Fig. 5. Pyrolytical results of the bituminous sediment sample using the PAM : (a) A pyrogram of the
(a) A pyrogram of the original sample illustrating four peaks; (b) a pyrogram of
original sample illustrating four peaks; (b) a pyrogram of the solvent Microcline (KAlSi
extracted O ) demonstrating only 1
sample
3 8
the solvent extracted sample demonstrating only the late peak, indicating kerogen
the bitumen;
or solid late peak, indicating
(c) a pyrogram kerogen
of the or solid
diesel sample; bitumen;
and (d) the combined (c) a pyrogram of the diesel
Halite (NaCl) sample; and (d) the 1
combined
diesel diesel
and extracted sampleand extracted
showing sample behavior
identical pyrolytical showing identical
of the original pyrolytical behavior of the original sample,
suggesting
sample, thatthethe
suggesting that original
original samplesample is aof mixture
is a mixture of diesel and indigenous
diesel and indigenous organic
Table 3. XRD analysis matter.
of the residual solids of the xylene treated bituminous
organic matter. sediment sample (type 1)
Table 4. Composition of the type 2 sludge sample 7 after XRF and XRD analyses
than bituminous coal. In this case, oil-based drilling will be Sample Saturates and Asphaltene
absorbed by the solid bitumen and make the substrate unsta- Resins (%)
Number Aromatics (%) (%)
ble and cause the bit to abort drilling. Water-based drilling 2 84.93 11.77 3.31
should be utilized to drill such formations.
3 64.19 20.22 15.59
The second type of sludge is characterized by soft appear-
ances and fine-grained sediments saturated by liquid hydrocar- 4 54.67 25.40 19.93
bon — a mixture of oil and diesel from drilling — and varies 5 33.60 40.74 25.66
inSample Number
color. The samples were Saturates and
assessed for Aromatics
their organic and(%) Resins
5 (%) Asphaltene
33.57 (%)40.82 25.61
2 84.93
inorganic composition utilizing pyrolysis, X-ray fluorescence 711.77 28.07 3.31 43.35 28.58
3
(XRF) and XRD techniques, respectively. 64.19
Sample number 20.22 15.59
4 54.67 25.40
Table 19.93
5. Saturates, aromatics, resin, and asphaltene data based on the pyrolysis of
2, which is brown in color, is rich in saturate and aromatic
5 33.60 the40.74
type 2 sludge samples 25.66
compounds
5 and have very low asphaltene contents unlike the
33.57 40.82 25.61
other
7 samples. Samples 3 and 4, which 28.07similar appear-
have measured
43.35 at 160 °F using 28.58various organic or inorganic acids
ances, have a higher abundance of saturates and aromatic and aliphatic or aromatic solvents, including sulfonic-based
Table 5. Saturates,
compounds compared toaromatics,
samples 5resin,
and 7.and asphaltene
Sample 7 was microemulsifying
data based surfactants.
on the pyrolysis of theMutual
type 2 solvents
sludgeand xylene
samples
selected for XRF and XRD analyses and illustrated dominance showed slight solubility values, i.e., 5 wt% to 19 wt%, with
of carbonate mineralogy, Table 4. The later samples have a the examined sludge samples. The solubility values were
high abundance of resin and asphaltene compounds, Table 5. slightly higher using mixtures of acetic and mutual solvents,
i.e., 17 wt% to 35 wt%, in samples 1 to 6, indicating the
Solubility Testing presence of acid soluble inorganic compounds, Fig. 6.
The dissolving power of formic acid is higher than ace-
The solubility of type 2 sludge samples — 1 to 7 — was tic acid. Therefore, the solubility values for samples 1 to 6
70 71
70 66 66
60 58
60 55 53 55
50 51 49
48 47 49
50 43
41 41
40 37 35 34 35
30 32 30
30 25 26 25
19 20 19 21
17 15 16 17
20 13 14
8 6
10 3 5
0
1 2 3 4 5 6 7
Sludge No.
Fig. 6. Solubility of the type 2 sludge samples in acids and solvents at 160 °F.
Fig. 6. Solubility of the type 2 sludge samples in acids and solvents at 160 °F.
Coreflood Testing
and CT Scan Analysis
Before After
Fig. 12. CT scan of core plug 1 before (left), and after (right) coreflood testing.
Fig. 12. CT scan of core plug 1 before (left), and after (right) coreflood t
CONCLUSIONS
Before
CT Distribution
ZULF-91 sandstoneX11244-246-275
S-1 sandstone^Stage-1213-214-220-244-246
246 246
After
ZULF-91 sandstoneX11244-246-275
246 i.e., 34 wt% to 55 wt%. Both acids were mixed with
either an ether-based mutual solvent or microemulsion
Fig. 11. CT scan of core plug 3 before (left), and after (right) coreflood testing.
solvent at 10 vol%.
Fig. 11. CT scan of core plug 3 before (left), and after (right) coreflood testing.
38 SPRING 2019 SAUDI ARAMCO JOURNAL OF TECHNOLOGY
• The microemulsifying surfactant showed no advantage in 2. Fink, J.K.: “Chapter 9, Filter Cake Removal,” in Petroleum
dissolving the type 2 sludge samples over the mutual sol- Engineer’s Guide to Oil Field Chemicals and Fluids, pp.
vent when mixed with formic acids. Therefore, utilizing a 295-309, Boston: Gulf Professional Publishing, 2012, 808 p.
mutual solvent in field treatment would be sufficient and 3. Jacobs, I.C.: “Chemical Systems for the Control of
cost-effective. Asphaltene Sludge during Oil Well Acidizing Treatments,”
• The highest solubility values were obtained with mixtures SPE paper 18475, presented at the SPE International
of 5 wt% HCl acid and solvents, showing solubilities be- Symposium on Oil Field Chemistry, Houston, Texas,
tween 79 wt% to 88 wt%. February 8-10, 1989.
4. Bustin, R.M.: Coal Petrology: Its Principles, Methods, and
• The solubility of the type 2 sludge samples — 1 to 6 — in
Applications, 2nd edition, Victoria, Canada: Geological
only 5 wt% HCl acid showed inconsistent results, i.e., 25
Association of Canada, 1985, 230 p.
wt% to 71 wt%, indicating that the presence of a mutual
solvent in the acid mixture is essential to maximize the 5. Taylor, G.H. and Glick, D.C.: Organic Petrology: A New
dissolutions of these sludge samples. Handbook Incorporating Some Revised Parts of Stach’s
Textbook of Coal Petrology, 4th edition, Berlin: Gebrüder
• The coreflood experiments utilizing HCl acid and formic
Borntraeger, 1998, 704 p.
acid mixtures showed a slight reduction in permeability
6. Sachse, V.F., Littke, R., Jabour, H., Schumann, T., et
— 20%.
al.: “Late Cretaceous (Late Turonian, Coniacian and
• The permeability of the core plugs were reduced slightly Santonian) Petroleum Source Rocks as Part of an OAE,
following injection of 3 PV of the 0.4 vol% cationic poly- Tarfaya Basin, Morocco,” Marine and Petroleum Geology,
meric clay stabilizer, indicating the clay stabilizer coated Vol. 29, Issue 1, January 2012, pp. 35-49.
minerals in the core plug.
7. Crelling, J.C. and Rimmer, S.M.: Crelling’s Petrographic
• Injection of HCl acid and formic acid mixtures or 10 Atlas of Coals and Carbons, Southern Illinois University
wt% formic acid in the presence of the 0.4 vol% clay sta- Carbondale Department of Geology, 2015, https://coaland-
bilizer showed a slight reduction in permeability by 5% carbonatlas.siu.edu.
to 13%.
• Although the coreflood experiments showed a slight
reduction in permeability, the CT scan results obtained
showed a significant increase in rock density along the
core length for core plugs 2 and 3, indicating the occur-
rence of chemical reactions with rock minerals that had
an insignificant impact in the core’s permeability.
ACKNOWLEDGMENTS
REFERENCES
Dr. Howard K. Schmidt, Jesus M. Felix Servin, and Dr. Erika S. Ellis
ABSTRACT INTRODUCTION
Proximity sensing was recently proposed as a way to simul- Long-term petroleum reservoir management ideally optimizes
taneously increase both range and resolution in cross-well production of oil while avoiding brine production, and mini-
electromagnetic (EM) tomography. The approach is applicable mizing well count and complexity. Given imperfect knowledge
to reservoirs with resistive seals. Earlier reports were based on of reservoir structures, significant inhomogeneity, and dynamic
finite element models of layered structures, with dielectric and multiphase fluid saturation, this is a difficult and long-stand-
conductivity contrasts matching those of known reservoirs. ing problem that would greatly reward improved methods for
Experimental work, now reported, is consistent with expec- observing the state and structure of the reservoir in near real-
tations based on finite element model simulations. Synthetic time. This is particularly true in the case of mature fields in
layered structures have been investigated using a 1.3 GHz secondary production on waterflood. Modern reservoir models
ground penetrating radar (GPR) system. A scaled reservoir derived from 3D seismic, well logs, and history matching are
model was constructed in a 1 m tank comprising sand filled certainly a vital tool for reservoir management.
with fluids of variable dielectric constant and conductivity. In Our lack of knowledge about large-scale inhomogeneity,
this system, dry sand, brine saturated sand, and a polymer including facture corridors, prevent anticipation of early
foam, provide a useful mimic for the electrical properties water breakthrough and bypass of significant volumes of
expected for a carbonate reservoir sealed by anhydrite. oil. As such, there is a great need for imaging tools that can
Data was recorded in the time domain using EM transients. locate flood fronts, detect bodies of bypassed oil, and map the
Observed trends in velocities and amplitude shifts were con- remaining oil column thickness across the entire reservoir with
sufficient resolution to guide key management decisions. Nat-
sistent with finite element models. Interestingly, polarization
urally, reservoir management would be easy if we had imag-
dependent signal transport first indicated by finite element
ing modalities with petrophysical scale resolution, e.g., well
modeling was supported by these experimental results.
logs ~0.1 m, over the available geophysical survey scales, e.g.,
Results to date indicate that greatly increased EM propaga-
seismic ~kilometers (km). Imaging resolution requirements
tion can be achieved through resistive geologic layers, rather
that can yield valuable and actionable information is probably
than directly through relatively conductive reservoir media.
much less challenging than that, and depends on the direction
We confirm that these layers act as planar transmission lines
and scale of the particular field under consideration.
and not as waveguides — meaning that there is no hard lower
For the purposes of this article, we will assert that for giant
cutoff frequency, and longer wavelengths can be used to sense
and super-giant fields (> 1 billion bbl), imaging modalities
and characterize reservoir fluids proximal to the dielectric
with resolution on the order of 1 m vertically, and up to sev-
channel. The results also confirm that variations in bounding
eral hundred meters laterally, could respectively determine
layers modulate the amplitude and velocity of the signal in
the remaining oil column and flooded/bypassed volumes with
the dielectric channel, and thereby demonstrate the concept of
sufficient accuracy to greatly improve reservoir management
proximity sensing.
practice and development planning. Historic approaches for
These results support a new technical direction for EM generating this kind of actionable information include direct
characterization of reservoirs, especially in conjunction with full volume imaging using acoustic and low frequency elec-
magnetic contrast agents, enabling efficient localization of tromagnetic (EM) probes. A new approach based on indirect
bypassed oil, and mapping the remaining oil columns in EM imaging via proximity sensing will be experimentally
mature reservoirs. described here.
Time (nS)
5.5
Material r r S/m 6
5
Wet Sand 14 1 ~1
(nS)
5.5
Transit
Dry Sand ~4 1 > 10-4 4.5
Transit Time
5
Foam 1.2 1 > 10-4
Channel Channel
4
4.5
Table 1. EM properties of materials comprising the reservoir model 3.5
4
used to mimic anhydrite as the EM channel with various 3
thicknesses — 10 cm to 25 cm. The EM channel was 60 cm 3.5 5 10 15 20 25
Channel Thickness (cm)
wide in all experiments and extended the full length of the
3
reservoir tank — 95 cm. EM transients were recorded with a 5
Fig. 2. Traveltime 10 of channel thickness
as a function 15 with the 20 25
E-field oriented vertically.
MALA ProEx GPR system using a pair (transmitter (Tx) and Channel Thickness (cm)
receiver (Rx)) of shielded separable microwave antennas. Each Fig. 2. Traveltime as a function of channel thickness with the E-field oriented
Fig. 2. Traveltime as a function of channel thickness with the E-field oriented vertically.
antenna includes a Wu-King Bow-Tie dipole antenna that vertically.
yields an overdamped two-cycle transient with a fundamental
6
frequency of 1.3 GHz — wavelength ~23 cm in free space.
The emitted frequency is polarized and propagates as trans- 5.5
TimeTransit
data were recorded at each station, and the ensemble was 5.5
4.5
Channel
arrival times. In this model system, the signal will propagate
Channel Transit
faster through the foam than the surrounding sand, due to the 3.5
4.5
sets for each were obtained with the electric field oriented 3.5
Channel Thickness (cm)
perpendicular or parallel to the plane of the EM channel. The Fig. 3. Traveltime as a function of channel thickness with the E-field oriented
3
first experiment varied the channel thickness, t, to study the horizontally.
Fig. 5
3. Traveltime 10 of channel thickness
as a function 15 20
with the E-field 25
oriented horizontally.
effect of the t/λ ratio. In the second, 2D tomograms (9 cm × 9 Channel Thickness (cm)
wavelength or greater, regardless of the polarization. Interest-
cm on 10 cm centers) were obtained across the channel with
ingly, the transit time increases — velocity decreases — when
left and right halves of the channel bounded by brine satu-
the 3.channel
Fig. thickness
Traveltime is less
as a function than thickness
of channel the wavelength for both
with the E-field oriented horizontally.
rated sand, and dry sand, respectively, to directly observe the
polarizations. In the vertical case, the signal is slowed by
proximity sensing effect, if any, and demonstrate the mapping
about 10% when the channel is less than about λ/2 (10 cm).
of the EM properties of the medium adjacent to the EM chan-
At λ/2, the channel is equivalent to a waveguide with nodes at
nel. Three different channel thicknesses were used: 10 cm, 15 each wall, but at λ/4 (5 cm), the wave is “forced” to sample
cm, and 20 cm. Tomograms were inverted from 81 individual the bounding medium.
transients using bh_tomo20. In all experiments, arrival times Consistent with our original hypothesis, the leaky bound-
for each transient were picked by hand. ary with a higher dielectric constant retards the wave and
increases transit time. The modest effect could indicate that
RESULTS AND DISCUSSION the electric field does not readily penetrate the relatively
conductive bounding medium, the brine filled sand. The
Effect of Channel Thickness retardation is profound for the horizontally polarized signal
— around a 60% increase in transit time with a λ/4 channel
In the first experiment, the channel thickness was varied from thickness. When the electric field is horizontal, the perpendic-
5 cm to 25 cm in 5 cm steps, to investigate the effect on signal ular magnetic component of the transverse EM wave is forced,
amplitude, and the speed of propagation. The (Tx) and (Rx) and indeed able, to enter and penetrate the conducive bound-
were located at the center of the channel on either side of the ing medium. This fascinating and unexpected result is reminis-
model, as previously shown in Fig. 1. Figures 2 and 3 show cent of birefringence of light in calcite crystals, which is due
the traveltime through the channel for vertical and horizontal to a varying velocity, depending on the polarization alignment
polarization, respectively. Since the channel has a dielectric with key crystal axes.
constant of 1.2, the 1.3 GHz probe has a wavelength of ~21 According to our hypothesis, by using a waveguide to
cm, and should have a velocity of ~3.3 nS/m. This indeed propagate EM signals with the λ comparable to channel
is just the observed velocity in channels comparable to that thickness, the energy will be contained within the channel
(log) 100000 Frequencies that result in wavelengths larger than the channel
10000
thickness will provide more information about the surround-
Signal Amplitude
1000
tunable frequency, and hopefully controllable polarization to
optimize the range while controlling sensitivity, and perhaps
1000 the depth of investigation into the reservoir.
100
5 10 15 20 25
Channel Thickness (cm) Tomography via Proximity Sensing
100
Fig. 4. Peak-to-peak
5 amplitude
10as a function of
15channel thickness
20 with the E-field
25 oriented vertically.
Our hypothesis also claims that changes in fluid saturation
Channel Thickness (cm)
and their specific EM properties in the reservoirs adjacent
Fig. 4. Peak-to-peak amplitude as a function of channel thickness with the E-field to vertically.
the channel will modulate the transported signal in either
Fig. 4. Peak-to-peak amplitude as a function of channel thickness with the E-field oriented
oriented vertically.
traveltime or amplitude, or both. To test this claim, the initial
100000 lab model was modified such that half of the channel was
covered with a layer of dry sand, Fig. 6. As before, multiple
layers of foam were used to vary the height of the channel to
(log)
100000
10000 include 10 cm, 15 cm, and 20 cm. If our approach is sensitive
Signal Amplitude
1000 and dry sand. For each channel thickness, 81 waveforms were
recorded by placing the Tx and the Rx in nine different posi-
tions each, in a tomographic manner, Fig. 7.
1000
100 Arrival times were picked manually and inversion was
5 10 15 20 25
done using the least squares approach in bh_tomo for each
Channel Thickness (cm)
100
different channel thickness. The output is a 2D velocity map
Fig.5.
Fig. 5.Peak-to-peak
Peak-to-peak
5 amplitude as aa function
10as
amplitude function of
15channel
of channel thickness
20 with
thickness withthe
theE-field
25 oriented horizontally.
E-field
oriented horizontally.
Channel Thickness (cm)
Fig. 8. The 10 cm channel inverted data. The left edge of the inversion corresponds
Fig. 8. The 10 cm channel inverted data. The left edge of the inversion corresponds
Fig. 7. Ray coverage from the 81 recorded waveforms. The left edge corresponds to the Rx
model. facetwo
The of the model. Theregions
contrasting two contrasting regions
correspond to correspond to wetvelocity
wet sand (high sand red region)
Fig. 7. Ray coverage from the 81 recorded waveforms. The left edge corresponds to the Rx side, and the
to the Rx side, and the signal propagates right to left. velocity blue red
(high velocity region) above
region) thesand
and dry channel.
(low velocity blue region) above the channel.
signal propagates right to left.
— of a higher field since the signal-to-noise ratio is propor- Oxford Instruments for the pore size distributions and verifi-
tional to the square root of the Larmor frequency. The signal cation. The NMR dispersion curves were obtained on all Sw
decays to a lower value corresponding to the relaxation field samples. Then the core samples were divided into two groups
instead of zero when there is no magnetic field. The FID of based on their mineralogy and pore size distributions with
both sequences is acquired at one constant acquisition field. each group containing one of the sister samples.
As can be seen from Figs. 1b and 1d, the FID at each Five pore volumes of mineral oil were injected through the
relaxation time was measured. The time to complete a whole Group 1 samples to reach irreducible water (D2O) satura-
NMR dispersion curve can be very lengthy, and range from tion, and D2O saturation with mineral oil and crude oil. The
10 to 20 hours, depending on the T1max. The τ can be equally samples of Group 2 were dried in the oven again at 110 °C
spaced in logarithmic and linear scales, respectively, while the overnight and saturated with mineral oil directly after being
logarithm concentrates on the short τ, and the linear on the in a vacuum. Then they were flooded with five pore volumes
longer τ. Estimated from the initial measurement, the τ can of crude oil. NMR dispersion curves were obtained at 100%
be customized to concentrate on the range of interest, which mineral and crude oil saturation.
saves time and improves efficiency. For samples with the short
T1, a logarithmic scale was used while for samples of medium
and long T1, a customized list focusing on the τ of interest was
used. There were either 30 equally spaced τ values for loga-
rithmic scale, or 28 τ values for the customized list, to cover
the whole gain or decay curves where the maximum τ equals
4*T1amx as default. Here, 25 or 30 frequencies were all equally
spaced in a logarithmic scale from 0.01 MHz to 18 MHz.
Experimental Procedure
(ml) (ml)
0.25
0.25
0.20 100%Sw BS3
100%Sw BS1
Volume
100%Sw BS1
135
(ml)
0.20 100%Sw BS3
0.20
0.15 100%Sw BS3 Data Analysis
Volume
100%Sw 135
Volume 0.25 100%Sw 135
0.15
Incremental
100%Sw BS1
(ml)
0.15
0.10 The software calculates the FID amplitudes by averaging the
0.20 100%Sw BS3
Incremental
100%Sw 135
0.10
0.05 tial fitting on the gain or decay curves. The NMR dispersion
0.15
0.05 curve is obtained by combining all single T1 at different relax-
0.05
0.00
Incremental
100%Sw IL703
(ml)
I3
0.20 100%Sw I2 sion of different pore systems is beyond the scope of this study.
Volume
0.20
0.15 100%Sw I2
100%Sw I3 As discussed in the introduction, Korb et al. (1997)5 and
Volume
0.25 100%Sw I3
Incremental
0.15 100%Sw IL703 Korb et al. (1999)6 proposed the relaxation models and
(ml)
0.15
0.10
obtained the correlation times by fitting the NMR dispersion
Incremental
0.20 100%Sw I2
Incremental
Volume
0.10 100%Sw I3 curves for the affinity index. The equations and derivation are
0.10
0.05
0.15 referred to in their studies5-7, 9, 10. Only a qualitative assessment
0.05
was performed due to the lack of necessary parameters.
Incremental
0.05
0.00
(b) 0.100.01 1 100 10000
0.00
0.000.01 T2 (ms) RESULTS AND DISCUSSION
(b) 1 100 10000
(b) 0.050.01 1 T2 (ms) 100 10000
T2 (ms) Core Sample Pore Structure by T2 Distributions
0.00
0.25
(b) 0.01 1
100%Sw 53
100 10000
0.25 The T2 distributions of the 100% DI Sw sample are illustrated
(ml) (ml)
T2 (ms)
0.25
0.20 100%Sw
100%Sw 92
53 in Fig. 3. They were divided into two groups, a single fluid,
Volume
100%Sw
100%Sw 53
100%Sw 131
(ml)
0.20 92 which was always 100% saturated with one fluid, and two
0.20
0.15 100%Sw 92
Volume
100%Sw
100%Sw 105
131 fluids, which was a D2O saturation after 100% Sw measure-
0.25
Volume
100%Sw 131
0.15 ment, so as to compare the NMR dispersion of the same flood
Incremental
100%Sw 105
53
0.15
(ml)
0.10
Incremental
Volume
0.10 100%Sw 131 are sister samples in Fig. 3a. Indiana limestone — I2 and I3
0.05
0.15 100%Sw 105 — are sister samples in Fig. 3b. They mainly have very similar
0.05
0.05
0.00 pore structures. Similarly, carbonates were paired according to
Incremental Volume (ml) Incremental
0.100.01 1 100 10000 the multiple modalities18. Samples 105 and 130, 131 and 128,
(c) 0.00
0.000.01 1
T2 (ms) 100 10000 53 and 65, 92 and 284, were selected as sister samples based
(c) 0.050.01 1 100 10000 on the pore structure shown in Figs. 3c and 3d, with similar
T2 (ms)
(c) 0.40 T2 (ms)
100%Sw 65
distributions. Sample 135 is a sandstone; Indiana limestone
0.00
0.35
100%Sw 128 IL703 is typically bimodal, which can be compared to carbon-
0.01 1 100 10000
(c) 0.30 100%Sw 130 ate samples of close pore systems. Sample 359 is a homoge-
T2 (ms)
100%Sw 284 neous limestone of low permeability.
0.25
100%Sw 359
0.20
NMR Dispersion of Bulk Fluids
0.15
0.10 The NMR dispersion curves of water, S3 mineral oil, and
0.05 crude oil are presented in Fig. 4a. The relaxation rates of DI
0.00 water and S3 mineral oil are 2.55 seconds and 0.48 seconds,
0.01 1 100 10000 respectively. They do not change with frequency as expected
(d) T2 (ms) in bulk liquids. The relaxation rate uniformity of DI water
and S3 mineral oil reflects the consistency and accuracy of
Fig. 3. T2 distributions of core samples: (a) sandstones, (b) limestones, (c) single measurements over the frequency range with nonpolarized
Fig.
fluid 3. T2 distributions
carbonates, of core
and (d) two fluid samples: (a) sandstones, (b) limestones, (c) single fluid carbonates, and (d)
carbonates.
two fluid carbonates. and polarized sequences. For example, the T1 values of DI
6 0.15
Deviation (1/s)
Bulk Oil Bulk S3 Water
5 packing, outcrop and low permeability reservoir carbonate
4 rocks,0.05
and fitted the data with respective equations. They
3 attributed the difference to be caused by “the ligand field
-0.05
2 between the proton molecular species and paramagnetic
1 -0.15 on the pore surface.” The affinity index, the ratio
impurities
0 -0.25 τS and 2D translational diffusion τm, is obtained
of residence
0.01 0.10 1.00 10.00 from the fitting using the equations. Other parameters such as
(a) Frequency (MHz) -0.35
surface density of paramagnetic impurities are needed for the
0.01 0.10 1.00 10.00
fitting, which are not currently available for all core samples
Fig. 4a. The NMR dispersion curves of bulk oil, S3 mineral oil, and water.
Fig. 4a. The NMR dispersion curves of bulk oil, S3 mineral oil, andto (b)obtain the affinity index.Frequency
water. The affinity(MHz)
index can be still
0.35 assessed qualitatively from the NMR dispersion since the large
Fig.
slope4b. The deviation
indicates values of
a large affinity DI water.
index or water wetness for the
0.25
same types of samples in these studies.
0.15 In Fig. 5b, the NMR dispersion of all samples are
Deviation (1/s)
-0.25 25
BS1 Sw BS3 Sw
135 Sw I2 Sw
-0.35 I3 Sw IL703 Sw
0.01 0.10 1.00 10.00 20 65 Sw 92 Sw
53 Sw 105 Sw
(b) Frequency (MHz) 128 Sw 130 Sw
1/T1 (1/s)
15 131 Sw 284 Sw
Fig. 4b. The deviation values of DI water. 359 Sw Water
Fig. 4b. The deviation values of DI water.
water mostly fall into the range of 2.55 ± 0.05 seconds, indi- 10
cated in Fig. 4b. The T1 log mean of the S3 mineral oil is 0.50
seconds by saturation sequence, and 0.53 seconds by inversion 5
sequence using 12.8 MHz spectrometers.
As shown from the oil NMR dispersion trend line, the 0
NMR dispersion of crude oil has a logarithmic frequency 0.01 0.10 1.00 10.00
dependency
25 indicating a small amount of asphaltene present (a) Frequency (MHz)
BS1 Sw BS3 Sw
in this crude14. Korb et al. (2013)14 obtained the residence
135 Sw I2 Sw and Fig. 5a. The NMR dispersion of 15 core samples at 100% Sw.
I3 Sw
translational τm using the equation derived
2D 20 IL703 Sw
from asphal- Fig. 5a. The NMR dispersion of 15 core samples at 100% Sw.
65 Sw 92 Sw
tene aggregates surface relaxation model similar
53 Sw to the
105rock
Sw
25
128 Sw 130 Sw BS3 S3 I2 S3
surface. The asphaltene effect will be present for NMR dis-
1/T1 (1/s)
15 131 Sw 284 Sw 53 S3 92 S3
359 Sw Water
persion of the crude oil in the cores. It needs to be considered 20
105 S3 BS3 So
I2 So 53 So
when10 analyzing the NMR dispersion of core samples to obtain 105 So 92 So
Bulk Oil Bulk S3
the net rock surface effect.
1/T1 (1/s)
15
5
100% Saturated with a Single Phase Fluid
10
0
The NMR
0.01 dispersion 0.10
of 15 core samples
1.00at 100% Sw10.00
and
5
bulk Frequency
(a) water are illustrated in Fig. 5a. (MHz)
The NMR dispersion of
five core samples at 100% S3 mineral oil saturation, and five
0
Fig. 5a. The
samples NMR crude
at 100% dispersion of 15 core
oil saturation aresamples at 100%
illustrated in Fig. Sw. 0.01 0.10 1.00 10.00
5b, along with bulk S3 mineral and crude oil. (b) Frequency (MHz)
In Fig. 5a, most samples — Samples BS1, BS3, I2, I3,
Fig. 5b. The NMR dispersion of samples at 100% saturation with a single fluid.
92, 105, 128, 130, 131, 284, and 359 — appear to be Fig. 5b. The NMR dispersion of samples at 100% saturation with a sin
1/T1 (1/s)
15
crude oil saturations are the largest among the carbonate sam-
ples, and all samples. It might contain a higher percentage of
10
paramagnetic impurities. The NMR dispersion slopes of the
100% crude oil saturated carbonate samples are comparable
5
to the ones of 100% Sw, considering the NMR dispersion of
crude oil with a trend line in the graph. For sister samples, the
0
Berea sandstones — BS1 and BS3 — and Indiana limestones
0.01 0.10 1.00 10.00
— Sample I2 and I3 — their slopes of 100% Sw and crude oil (a) Frequency (MHz)
saturation are similar.
It is interesting to compare the NMR dispersion of 100% Fig. 6a. The NMR dispersion for the Berea and Indiana sandstone samples at
Fig. 6a. The NMR dispersion for the Berea and Indiana sandstone samples
D2O saturation.
Sw and crude oil saturation among sample groups and sister
samples for understanding wettability, which indicates the 25 65 SirS3 65 SirSo
rock surface preference to different fluids. For example, the 128 SirS3 128 SirSo
130 SirS3 130 SirSo
Berea sandstones are known to be typically water-wet, and 20 284 SirS3 284 SirSo
Indiana limestones are intermediate wet or weakly water-wet. 359 SirS3 359 SirSo
Bulk S3 Bulk Oil
1/T1 (1/s)
The water affinity of Indiana limestone — Samples I2 and I3 15
— is even slightly larger than the Berea sandstones — Samples
BS1 and BS3 — from 100% Sw. What may render the Berea
10
sandstones more water-wet than Indiana limestone is their
small oil affinity indicated by Sample BS3 at 100% S3 mineral
5
oil saturation and Sample BS1 at 100% crude oil saturation.
Another example is the comparison between two carbonate
0
samples — Samples 53 and 105 — which have NMR dis- 0.01 0.10 1.00 10.00
persion of all three fluids at 100% saturation. Their NMR (b) Frequency (MHz)
dispersion at 100% S3 mineral oil and crude oil saturation
Fig. 6b. The NMR dispersion of the carbonate samples saturated with bulk
are very close, and a larger slope of Sample 105 at 100% Sw
mineral and crude oil.
indicates its more water-wet than Sample 53. The quantitative Fig. 6b. The NMR dispersion of the carbonate samples saturated with bulk
comparison can be performed from the affinity index calcula- to the ones in Fig. 5b.
tion in a future study. For crude oil samples, some samples agree with the above
assumption, such as Samples 284, BS1, 135, and 284, which
D2O Saturation indicates a smaller oil affinity index. Some samples, such as
Samples 65, 130, and 359 have comparable slopes, and others
Figure 6a shows the NMR dispersion for the Berea and Indian such as Samples I3 and 284 have larger slopes approaching
sandstone samples at D2O saturation. Figure 6b shows the 100% crude oil, and are larger than the average of four car-
NMR dispersion of the carbonate samples saturated with bulk bonates previously seen in Fig. 5b. The slopes of IL703 at
mineral and crude oil; trend lines are shown for comparison. 100% Sw and D2O with crude oil are close, and they are the
They were obtained after oil flood without an extended aging largest among all samples. It appears that paramagnetic impu-
period. The NMR dispersion was from mineral oil and crude rities somehow tend to interact with protons relaxation rather
oil, as D2O was used as a water phase. The study will continue effectively despite D2O.
monitoring any changes with time, and water may be intro-
duced for the NMR dispersion of a water phase at the end. CONCLUSIONS
Since the mineral oil was injected into 100% D2O saturated
samples, it does not contact all rock surfaces in the presence NMR dispersion was obtained from core samples of different
of water despite the wettability. It is expected that the NMR mineralogy and pore types at various saturation states. The
dispersion of both mineral and crude oil fall between bulk oil wettability of common types of cores selected was analyzed
without the effect of a rock surface, and 100% oil saturation based on their affinity to water and oil from the assessment of
with the full effect of a rock surface. The results do not fully their NMR dispersion at various saturation states. The follow-
verify this assumption. It is not obvious for the S3 mineral oil ing conclusions can be drawn from the current study on the
samples due to the small slopes; however, they are comparable core sample selected:
DATA ANALYSIS
Depth (m)
Depth (m)
-2040.00 -2040
a marked anisotropy (azimuthal
variation) exists from the W to the
-2060.00 -2060
E directions relative to the well.
This pattern is in very good agree-
-1980.00 -1980
2,399 m 3,076 m ment with the saturation estimates
-2080.00
1,803 m -2080
2,496 m
1,281 m 1,900 m
provided by the reservoir simula-
(a) Hz (b) 634 m Ez (c) 1,377 m tor. Similar spatial variations are
-2000.00 -2000
-2100.00
1.0E-09
1.00E-09 1.0E-08
1.00E-08 1.0E-07
1.00E-07 1.0E-06 1.00E-05 1.0E-12 1.0E-11 1.0E-10 1.0E-09 1.0E-08
1.00E-06 1.0E-05
-2100
11 10
10 100
100 1000
1000
observed in the vertical Ez ampli-
20 m
Fig. 5. Comparison of field measurements vs. parameter variations in the reservoir section, including: (a) Hz amplitude at are much smoother and lower
Fig. 5. Comparison
various Tx offsets, (b) of vertical
field measurements
Ez amplitude at vs. parameter
various Tx offsets,variations in the reservoir
and (c) induction section,
log resistivity including:
(continuous (a)with
curve)
amplitude, though they still cor-
Depth (m)
Depth (m)
Hzreconstructed
amplitude at various Tx offsets, (b) vertical Ez amplitude at various Tx offsets, and (c) induction log
resistivity from vertical Ez measurements (dashed line).
resistivity (continuous curve) with reconstructed-2040.00 resistivity from vertical Ez measurements (dashed line). relate well with estimated -2040
reservoir
source and receiver locations 4, 10
it is clear the measured verti- saturation variations. These observations are in agreement
cal Ez is primarily influenced by the reservoir resistivity struc- with the results of the modeling study on the same well, which
-2060.00 -2060
ture at the well position. Using a reference resistivity of a ver- concluded that the only EM field with enough signal-to-noise
tical Ez logged section beneath the reservoir, we can calibrate to map reservoir saturation variations in the reservoir was the
the relative vertical Ez variations and reconstruct -2080.00 the reservoir vertical Ez4. -2080
20 m
20 m
able baseline resistivity distribution, the time-related changes -2000
Amp_Rep
Depth (m)
ervoir management. Effectiveness of time-lapse observations -2040
Depth
Depth
are inherently related to the amount of signal and amount of
noise in the measurements that are also related to the rate of -2060
of four days from a Tx position at 2.3 km from the well. The Amplitude (V/m)
Amplitude (V/m) Phase (deg)
vertical Ez profiles in terms of amplitude and phase indicate Fig. 7. Repetition of the vertical Ez depth profile from a Tx distance of 2.3 km
overall good repeatability of the measurements, Fig. 7, where Fig. 7. Repetition
from of the
the well. The vertical
lower part E depth
ofz the profile
well from aby
is affected Txwashout
distanceand
of 2.3 km larger
shows from the well. The
of repetition
the well iserrors.
affected by washout and shows larger repetition errors.
the upper section of the well performed better — 0.3% error
in log amplitude and 1.2% error in phase — than the lower for vertical Ez measurements13. Other sources of measure-
interval — 0.4% error in log amplitude and 4.7% error in ment errors can be related to depth errors in the positioning
phase — where the caliper information indicated the presence of the wireline tool (currently estimated to be a few tens of
of a washout. The wellbore rugosity may have influenced the cm), intrinsic instrumentation noise and possible variations
repeated measurements by tilting of the electrode assemblage in the well fluids over time. During the survey, the well fluids
that is galvanically coupled to the borehole walls by means of were slowly depleting and required repeated pumping opera-
metal centralizers. Verticality is a very important prerequisite tions. Tilting, depth errors, and fluid composition variations Chart T
10
threshold
% of Data
6 Modeled time-lapse
signal: 2 years
4
Modeled time-lapse
signal: 5 years
2
Depth
0
Depth
(c)
(b) 1.0E-14
1E-14 1.0E-13
1E-13 1.0E-12
1E-12 1.0E-11
1E-11 1.0E-10
1E-10 1.0E-09
1E-09
Amplitude
Amplitude (V/m) (V/m)
Chart Title
Fig. 8. Time-lapse electric field signal variations as a result of waterflooding (modeled data) vs. the vertical Ez amplitude repetition error as measured in the well: (a)
histogram
10
showing the variations of the vertical Ez signal over 2 and 5 years of waterflooding from modeling4; (b) maximum field strength variations; and (c) comparison
between repetition error and time-lapse field strength variations.
Amp_diff
Estimated noise
20 m
signal: 2 years
can be modeled to obtain estimates of their impact on the 1.E-07
measurements.
The repetition errors in the vertical Ez are then compared
to the estimated signal changes estimated from reservoir sim- 1.E-08
ulator modeling4. The calculated 2-year and 5-year time-lapse
vertical Ez signal, normalized by the source moment and by
the receiver electrode separation, is then compared to the
Amplitude (V/m)
1.E-09
amplitude differences from the repeated measurements, Fig.
8. A few observations can be made. The measurement noise
threshold in the Colombo and McNeice (2013)4 study is esti-
1.E-10
mated at 1E-12 V/m, Fig. 8a, which corresponds to the small-
Semi-analytical open (70m)
est error in the repeated measurements, Fig. 8c. The time- Semi-analytical cased (70m)
lapse signal due to waterflooding is estimated to be above Semi-analytical cased (20m)
1.E-11
the repetition noise after 2 years in the lower portion of the FD open (70m)
FD cased (70m)
reservoir, and substantially above the time-lapse noise after
FD cased (20m)
5 years, Figs. 8b and 8c, except where the measurements are
1.E-12
influenced by the presence of casing. The repeatability analy- 100 1000
sis suggests that the time-lapse measurements should be able Offset (m)
to provide the requested information about the waterfront
Fig. 10. Plot of the modeled CSEM amplitude for receivers at 20 m and 70 m
evolution. Fig. 10.
below thePlot of shoe
casing the modeled
for varyingCSEM amplitude for receivers at 20 m and 70 m below
Tx offset.
varying Tx offset.
DATA INTERPRETATION WORKFLOW solutions are currently being explored. Figure 10 compares the
responses of the semi-analytical solution11 with an FD solution
Having assessed the signal-to-noise and repeatability of the obtained by embedding the casing in the model. The calcu-
surface-to-borehole measurements, we now identify the key lation is performed for a reservoir without casing and with
steps to derive a robust estimate of 3D resistivity distribution. casing at an increasing Tx distance from the well, and for dif-
An analysis of the processing steps for data conditioning ferent measurement depths in the reservoir, corresponding to
leading to the final 3D inversion is shown in Fig. 9. Some of an increasing distance from the casing shoe. The FD approach
the most important aspects in this workflow are modeling the matches perfectly with the semi-analytical solution when the
steel casing effect and the strategies to account for it in the casing is not present and tends to approximate the semi-ana-
data. Steel casing has a strong signature on the measurement lytical solution as a function of the Tx distance and depth of
of the borehole’s vertical Ez, and strategies for dealing with it observation in the reservoir when the casing is considered. At
range from embedding a scaled up representation of the casing -70 m from the casing shoe, the FD solution is valid for Tx
directly into the model using the material property mapping offsets greater than 500 m, while at -20 m from the casing
theory and FD or finite element numerical methods12, 14, 15, or shoe, the FD response matches the semi-analytical solution
by modeling and subtracting its effects from the data using only when the transmitter is beyond 2 km from the well.
semi-analytical solutions9. Here we have opted for a numeri- Galvanic distortions can occur at the source electrode sites.
cal representation of the casing effect modeling it by directly These effects are described as a local accumulation of charges
using a FD scheme while finite element and semi-analytical caused by 3D heterogeneous resistivity distributions in the
near surface and typically referred to as vertical Ez “statics.”
Such effects are well-known in MT and land CSEM measure-
ments, and techniques to remove them based on magnetic
induction methods are described in the literature16, 17. The ver-
tical Ez data measured in the borehole are well behaved show-
ing a smooth azimuthal variation, suggesting that, if present,
such galvanic distortion effects are of minor concern and
could be dealt with directly in the inversion phase by solving
for additional free parameters representing statics15.
The last preparatory phase leading to the 3D inversion con-
sists of overburden characterization. The 3D surface-to-bore-
hole CSEM inversion problem is typically underdetermined
Fig. 9. Data interpretation workflow highlighting the key data conditioning and with a much larger number of unknowns than observations.
model building steps to enable robust 3D inversions of the surface-to-borehole Such an inverse problem can be solved only by the introduc-
CSEM data set.
tion of constraints. The reservoir section is the target of the
100 m
the reservoir resistivity distribution that represents the baseline
100 m
Depth (m)
physics and/or structure operators. The external regularization
can be embedded in the inversion procedure in a Bayesian
Depth (m)
3D INVERSION
Kimon N. Alexandrou
Since the company’s first patent in 1950, Saudi Aramco has efficiencies in our chemicals business.
contributed significantly to the world’s innovation efforts with Supporting the company’s commitment to creating a robust
high-value intellectual property (IP), which has positioned the portfolio of IP, the network innovation model that facilitates
company as a leader in the energy sector. strategic alliances with world-class organizations has proven
In 2018, Saudi Aramco achieved its best year yet, with 309 successful in enabling Saudi Aramco to enhance its compet-
granted patents from the United States Patent and Trademark itiveness, and expand its global technology footprint. These
Office, which put the company second among oil and gas collaborations have contributed to the rise in the number
companies worldwide in the number of patents granted for of patented technologies that have been developed between
the year. Saudi Aramco and our partners, including leading technical
A well-developed IP portfolio supports Saudi Aramco’s innovators in the industry, as well as leading academic
competitive advantage, validates the contributions made institutions in-Kingdom and around the world.
by our scientists and researchers, solidifies our position
as a technology leader in the energy and chemicals fields,
and provides commercialization opportunities for non-core
technologies. Patents provide value to the company and
the Kingdom of Saudi Arabia by enabling Saudi Aramco to
deploy these technologies without the fear of competitors
taking the idea and deploying the same or similar
technology. To maximize value for the business, only globally
competitive technologies are being developed and deployed,
affording Saudi Aramco a continued leadership advantage.
Recent published research from Stanford University has
found that there are vast differences in the carbon intensity of
global upstream operations. Technology governance in drilling
and reservoir management are at the heart of operations,
sustaining the production of one of the lowest carbon
intensities of a barrel of oil equivalent produced globally. At
Saudi Aramco, technology is the enabler, and central to our
ability to reduce greenhouse gas emissions from across our
operations.
From the creation of the Master Gas System in the 1970s
that has virtually eliminated flaring in Saudi Arabian oil
fields, to methane reduction, to carbon capture, utilization
and storage, and to fuel engine matching initiatives in
transportation, innovations are making a meaningful
difference below and above the ground.
For downstream, our research and development activities
seek to develop and implement process improvement and
production efficiencies in support of the company’s growing
petrochemicals business. The direct conversion of crude
oil to petrochemicals is a single step process, and is both a
promising and significant development that will deliver higher
Catalysts and Methods for Polymer Synthesis Scissor-Mechanism Closing Rams of Blow Out Preventers
Granted Patent: U.S. Patent 9,856,349, Grant Date: January 2, 2018 Granted Patent: U.S. Patent 9,869,149, Grant Date: January 16, 2018
Jay J. Farmer Mohammad S. Al-Badran
Header for Air Cooled Heat Exchanger Kalina Cycle-based Conversion of Gas Processing Plant Waste
Granted Patent: U.S. Patent 9,857,127, Grant Date: January 2, 2018 Heat into Power
Dhawi A. Al-Otaibi Granted Patent: U.S. Patent 9,869,209, Grant Date: January 16, 2018
Mohammad S. Al-Badran
Systems and Methods for Near Infrared-based Water Cut
Monitoring in Multiphase Fluid Flow Nano-Level Evaluation of Kerogen-Rich Reservoir Rock
Granted Patent: U.S. Patent 9,857,298, Grant Date: January 2, 2018 Granted Patent: U.S. Patent 9,869,649, Grant Date: January 16, 2018
Muhammad Arsalan, Talha J. Ahmad, and Mohamed N. Noui-Mehidi Katherine L. Hull, Younane N. Abousleiman, and Sebastian Csutak
Cyclone Separation and Recovery of Carbon Dioxide from Method for Non-Intrusive Measurement of Low Water Content
Heated Liquid Absorbent in Oil
Granted Patent: U.S. Patent 9,861,910, Grant Date: January 9, 2018 Granted Patent: U.S. Patent 9,869,664, Grant Date: January 16, 2018
Ahmad D. Hammad, Abdulrahman Z. Akhras, Zaki Yusuf, Nayif A. Ezzat M. Hegazi and Abdul-Rahman Z. Akhras
Rasheedi, and Abdullah M. Al-Qahtani
Dual-Phase Acid-based Fracturing Composition with Corrosion
High Temperature Fracturing Fluids with Nano-Crosslinkers Inhibitors and Method of Use Thereof
Granted Patent: U.S. Patent 9,862,878, Grant Date: January 9, 2018 Granted Patent: U.S. Patent 9,873,829, Grant Date: January 23, 2018
Ghaithan A. Al-Muntasheri, Feng Liang, Hooisweng Ow, Jason Cox, Saleh H. Al-Mutairi, Yaser K. Al-Duailej, Ibrahim S. Al-Yami,
and Martin E. Poitzsch Abdullah M. Al-Hajri, and Hameed Al-Badairy
Chemical-based Well Kickoff System for Naturally Flowing Reversible Aminal Gel Compositions, Methods, and Use
Wells
Granted Patent: U.S. Patent 9,879,170, Grant Date: January 30, 2018
Granted Patent: U.S. Patent 9,863,226, Grant Date: January 9, 2018
Peter J. Boul, B. Raghava Reddy, Matthew Hilfiger, and Carl J.
Rafael A. Lastra and Mohammed N. Noui-Mehidi Thaemlitz
Fracturing Fluid for Subterranean Formations Integrated Ebullated Bed Hydroprocessing, Fixed Bed
Granted Patent: U.S. Patent 9,863,231, Grant Date: January 9, 2018 Hydroprocessing and Coking Process for Whole Crude Oil
Conversion into Hydrotreated Distillates and Petroleum
Katherine L. Hull, Mohammed Sayed, and Ghaithan A. Al-Muntasheri
Green Coke
Granted Patent: U.S. Patent 9,879,188, Grant Date: January 30, 2018
High Efficiency Solar Power Generator for Offshore
Applications Omer R. Koseoglu
Granted Patent: U.S. Patent 9,863,404, Grant Date: January 9, 2018
Recovery and Re-Use of Waste Energy in Industrial Facilities
Michael J. Black and Abubaker S. Saeed
Granted Patent: U.S. Patent 9,879,918, Grant Date: January 30, 2018
Systems and Methods for Monitoring Casing Cement Integrity Mahmoud B. Noureldin and Hani M. Al-Saed
Granted Patent: U.S. Patent 9,863,895, Grant Date: January 9, 2018
Dual Catalyst System for Propylene Production
Shouxiang Ma, Darryl Trcka, and Robert Wilson
Granted Patent: U.S. Patent 9,884,794, Grant Date: February 6, 2018
Modular Mobile Inspection Vehicle Sulaiman S. Al-Khattaf, Arudra Palani, Tazul I. Bhuiyan, Mohammad
N. Akhtar, Abdullah M. Aitani, Mohammed A. Al-Yami, and Sohel
Granted Patent: U.S. Patent 9,863,919, Grant Date: January 9, 2018 Shaikh
Pablo Carrasco Zanini, Ali Outa, Fadl H. Abdel Latif, Brian J.
Parrott, Hassane Trigui, Sahejad Patel, and Ayman Amer Polymer Compositions and Methods
Granted Patent: U.S. Patent 9,884,937, Grant Date: February 6, 2018
Aliphatic Polycarbonate Quench Method
Wayne R. Willkomm and Scott D. Allen
Granted Patent: U.S. Patent 9,868,816, Grant Date: January 16, 2018
Jeffrey R. Conuel, David E. Decker, Scott D. Allen, and Anna E. Cement Oil-based Mud Spacer Formulation
Cherian
Granted Patent: U.S. Patent 9,884,985, Grant Date: February 6, 2018
Integrated Hydrotreating and Isomerization System with Mohammad L. Al-Subhi, Ahmad S. Al-Humaidi, and Scott S. Jennings
Aromatic Separation
Granted Patent: U.S. Patent 9,868,914, Grant Date: January 16, 2018
Omer R. Koseoglu
Granted Patent: U.S. Patent 9,890,632, Grant Date: February 13, 2018,
Apparatus, Computer Readable Medium, and Program Code
Shouxiang Ma, Ali R. Belowi, and Darryl Trcka for Evaluating Rock Properties while Drilling Using Downhole
Acoustic Sensors and Telemetry System
Recovery and Re-Use of Waste Energy in Industrial Facilities Granted Patent: U.S. Patent 9,903,974, Grant Date: February 27, 2018
Granted Patent: U.S. Patent 9,891,004, Grant Date: February 13, 2018 Yunlai X. Yang
Mahmoud B. Noureldin and Hani M. Al-Saed
Integrated Process for Producing Anode Grade Coke
Stand-alone Portable Sensing System for Advanced Granted Patent: U.S. Patent 9,909,068, Grant Date: March 6, 2018
Nanoparticle Tracers
Omer R. Koseoglu
Granted Patent: U.S. Patent 9,891,170, Grant Date: February 13, 2018
Erika S. Ellis Integrated Process for in Situ Organic Peroxide Production
and Oxidative Heteroatom Conversion
Highly Selective Polynorbornene Homopolymer Membranes Granted Patent: U.S. Patent 9,909,074, Grant Date: March 6, 2018
for Natural Gas Upgrading Omer R. Koseoglu and Abdennour Bourane
Granted Patent: U.S. Patent 9,896,527, Grant Date: February 20, 2018
Benjamin J. Sundell and John A. Lawrence Staged Chemical Looping Process with Integrated Oxygen
Generation
Processes and Systems for Fluidized Catalytic Cracking Granted Patent: U.S. Patent 9,909,756, Grant Date: March 6, 2018
Granted Patent: U.S. Patent 9,896,627, Grant Date: February 20, 2018 Tidjani Niass and Mourad V. Younes
Omer R. Koseoglu
Process to Upgrade and Desulfurize Crude Oil by
Integrated Process to Produce Asphalt, Petroleum Green Coke, Supercritical Water
and Liquid and Gas Coking Unit Products Granted Patent: U.S. Patent 9,914,885, Grant Date: March 13, 2018
Granted Patent: U.S. Patent 9,896,629, Grant Date: February 20, 2018 Ki-Hyouk Choi, Joo-Hyeng Lee, and Mohammad S. Garhoush
Omer R. Koseoglu
Integrated Pump and Compressor and Method of Producing
Inflow Control System for Use in a Wellbore Multiphase Well Fluid Downhole and at Surface
Granted Patent: U.S. Patent 9,896,905, Grant Date: February 20, 2018 Granted Patent: U.S. Patent 9,915,134, Grant Date: March 13, 2018
Using Radio Waves to Fracture Rocks in a Hydrocarbon Recovery and Re-Use of Waste Energy in Industrial Facilities
Reservoir Granted Patent: U.S. Patent 9,915,477, Grant Date: March 13, 2018
Granted Patent: U.S. Patent 9,896,919, Grant Date: February 20, 2018 Mahmoud B. Noureldin and Hani M. Al-Saed
Jin-Hong Chen, Daniel T. Georgi, and Hui-Hai Liu
Supercritical Reactor Systems and Processes for Petroleum
Three-Dimensional Reservoir Pressure Determination Using Upgrading
Real Time Pressure Data from Downhole Gauges Granted Patent: U.S. Patent 9,920,258, Grant Date: March 20, 2018
Granted Patent: U.S. Patent 9,896,930, Grant Date: February 20, 2018 Ki-Hyouk Choi, Abdullah T. Alabdulhadi, and Mohammed A.
Alabdullah
Omar A. Al-Nahdi, Sami A. Al-Nuaim, Alan L. Siu, and Ahmad T.
Al-Shammari
Selective Series-Flow Hydroprocessing System
Granted Patent: U.S. Patent 9,920,265, Grant Date: March 20, 2018
Omer R. Koseoglu
Apparatus, Method and System for Detecting Salt in a Integrated Calcium Looping Combined Cycle for Sour Gas
Hydrocarbon Fluid Applications
Granted Patent: U.S. Patent 9,939,405, Grant Date: April 10, 2018 Granted Patent: U.S. Patent 9,951,689, Grant Date: April 24, 2018
Naim Akmal, Rashed M. Aleisa, and Milind M. Vaidya Mourad Younes, Ali Hoteit, and Aqil Jamal
Evaluating Effectiveness of Ceramic Materials for Preparation and Use of Drilling Fluids with Date Seed Powder
Hydrocarbons Recovery Fluid Loss Additive
Granted Patent: U.S. Patent 9,939,421, Grant Date: April 10, 2018 Granted Patent: U.S. Patent 9,957,433, Grant Date: May 1, 2018
Sameeh I. Batarseh, Hazim H. Abass, and Ayman R. Al Nakhli Md. Amanullah, Jothibasu Ramasamy, Turki Alsubaie, and Omar
Fuwaires
Systems, Methods, and Computer Medium to Produce
Efficient, Consistent, and High Confidence Image-based Petroleum Upgrading Process
Electrofacies Analysis in Stratigraphic Interpretations Across Granted Patent: U.S. Patent 9,957,450, Grant Date: May 1, 2018
Multiple Wells
Ki-Hyouk Choi, Ashok K. Punetha, Mohammed R. Al-Dossary, and
Granted Patent: U.S. Patent 9,939,548, Grant Date: April 10, 2018 Sameer A. Al-Ghamdi
Gordon Burmester and Keith A. Macpherson
Two-Step Process for Aromatics Production from Natural Gas/
Enhancement of Claus Tail Gas Treatment with Membrane Shale Gas Condensates
and Reducing Step Granted Patent: U.S. Patent 9,957,451, Grant Date: May 1, 2018
Granted Patent: U.S. Patent 9,943,802, Grant Date: April 17, 2018 Raed Abudawoud
Feras Hamad, Milind M. Vaidya, Jean-Pierre Ballaguet, Sebastien A.
Duval, and Iran D. Charry-Prada Adjusting a Fuel On-Board a Vehicle
Granted Patent: U.S. Patent 9,957,903, Grant Date: May 1, 2018
Method for Reducing Fluid Loss during Drilling of a
Hydrocarbon Formation Using a Water-based Drilling Esam Z. Hamad and Ibrahim M. Al-Gunaibet
Fluid Composition Having a Multifunctional Mud Additive
Granted Patent: U.S. Patent 9,944,841, Grant Date: April 17, 2018 Line Blind Valve Assembly Having an Injection Sealing System
Md. Amanullah and Mohammed K. Al-Arfaj Granted Patent: U.S. Patent 9,958,072, Grant Date: May 1, 2018
Omar M. Al-Amri
Apparatus, Method and System for Detecting Salt in a Methods for Evaluating Rock Properties while Drilling
Hydrocarbon Fluid Using Drilling Rig Mounted Acoustic Sensors
Granted Patent: U.S. Patent 9,970,895, Grant Date: May 15, 2018 Granted Patent: U.S. Patent 9,989,661, Grant Date: June 5, 2018
Naim Akmal, Rashed M. Aleisa, and Milind M. Vaidya Yunlai Yang and Yi Luo
Claus Process for Sulfur Recovery with Intermediate Water System and Method for Generating Power and Enhanced
Vapor Removal by Adsorption Oil Recovery
Granted Patent: U.S. Patent 10,005,666, Grant Date: June 26, 2018 Granted Patent: U.S. Patent 10,014,541, Grant Date: July 3, 2018
Cemal Ercan, Rashid M. Othman, and Yuguo Wang Aqil Jamal, Thang V. Pham, and Aadesh Harale
Propylene Production Using a Mesoporous Silica Foam Gas Separation Membrane Module for Reactive Gas Service
Metathesis Catalyst Granted Patent: U.S. Patent 10,016,728, Grant Date: July 10, 2018
Granted Patent: U.S. Patent 10,005,703, Grant Date: June 26, 2018 Sudhir S. Kulkarni, Karl S. Beers, Jean-Pierre R. Ballaguet, Milind M.
Raed Abudawoud, Sulaiman S. Al-Khattaf, Arudra Palani, Tazul Vaidya, and Sebastien A. Duval
I. Bhuiyan, Mohammad N. Akhtar, Abdullah M. Aitani, and
Mohammed A. Al-Yami Integrated Hydrotreating and Steam Pyrolysis System for
Direct Processing of a Crude Oil
Pendant Epoxide Polymers and Methods of Treating Granted Patent: U.S. Patent 10,017,704, Grant Date: July 10, 2018
Subterranean Formations
Raheel Shafi, Julio Hasselmeyer, Abdennour Bourane, Ibrahim A.
Granted Patent: U.S. Patent 10,005,930, Grant Date: June 26, 2018 Abba, and Abdul R.Z. Akhras
B. Raghava Reddy
Fast-Setting Retrievable Slim-Hole Test Packer and Method
System and Method for Fueling Alternative Fuel Vehicles of Use
Granted Patent: U.S. Patent 10,008,730, Grant Date: June 26, 2018 Granted Patent: U.S. Patent 10,018,039, Grant Date: July 10, 2018
Aqil Jamal and Thang V. Pham Shaohua Zhou
Process to Upgrade Highly Waxy Crude Oil by Hot Peristaltic Submersible Pump
Pressurized Water Granted Patent: U.S. Patent 10,018,193, Grant Date: July 10, 2018
Granted Patent: U.S. Patent 10,010,839, Grant Date: July 3, 2018 Rafael A. Lastra
Ki-Hyouk Choi, Khalid A. Al-Majnouni, and Ali Al-Shareef
Granted Patent: U.S. Patent 10,030,467, Grant Date: July 24, 2018
Magnetic Induction-based Localization for Wireless Sensor
Al-Waleed A. Al-Gouhi Networks in Underground Oil Reservoirs
Granted Patent: U.S. Patent 10,042,077, Grant Date: August 7, 2018
Well Testing through a Generated Exothermic Reaction
in the Wellbore Howard K. Schmidt, Ian F. Akyildiz, Shih-Chun Lin, and Abdullah A.
Shehri
Granted Patent: U.S. Patent 10,030,492, Grant Date: July 24, 2018
Ayman R. Nakhli, Hazim H. Abass, and Mirajuddin R. Khan High Strength Polyurethane Foam Compositions and Methods
Granted Patent: U.S. Patent 10,047,188, Grant Date: August 14, 2018
Systems, Methods, and Computer Medium to Provide
Scott D. Allen, Aisa Sendijarevic, and Vahid Sendijarevic
Entropy-based Characterization of Multiphase Flow
Granted Patent: U.S. Patent 10,030,511, Grant Date: July 24, 2018
Hydrocarbon Recovery Using Complex Water and Carbon
Talha J. Ahmad, Michael J. Black, Muhammad Arsalan, and Dioxide Emulsions
Mohamed N. Noui-Mehidi
Granted Patent: U.S. Patent 10,047,275, Grant Date: August 14, 2018
Systems, Methods, and Computer Medium to Provide Fawaz M. Al-Otaibi and Sunil L. Kokal
Entropy-based Characterization of Multiphase Flow
Granted Patent: U.S. Patent 10,030,512, Grant Date: July 24, 2018 Densifying Carbon Dioxide with a Dispersion of Carbon
Dioxide Philic Water Capsules
Talha J. Ahmad, Michael J. Black, Muhammad Arsalan, and
Mohamed N. Noui-Mehidi Granted Patent: U.S. Patent 10,047,276, Grant Date: August 14, 2018
Fawaz M. Al-Otaibi, Sunil L. Kokal, Howard K. Schmidt, and Yun
Characterization of an API Gravity Value of Crude Oil by Chang
Ultraviolet Visible Spectroscopy
Granted Patent: U.S. Patent 10,031,121, Grant Date: July 24, 2018 Non-Acidic Exothermic Sandstone Stimulation Fluids
Omer R. Koseoglu, Adnan Al-Hajji, and Gordon Jamieson Granted Patent: U.S. Patent 10,047,277, Grant Date: August 14, 2018
Mohammad N. Al-Dahlan, Ayman R. Al-Nakhli, and Abdullah M.
Al-Harith
Process for Maximizing Xylenes Production from Heavy
Aromatics for Use Therein
Granted Patent: U.S. Patent 10,035,742, Grant Date: July 31, 2018
Raed Abudawoud, Zhonglin Zhang, Qi Xu, and Ahmad A. Jazzar
Characterization of Crude Oil by Ultraviolet Visible Encapsulated Nanocompositions for Increasing Hydrocarbon
Spectroscopy Recovery
Granted Patent: U.S. Patent 10,048,194, Grant Date: August 14, 2018 Granted Patent: U.S. Patent 10,053,616, Grant Date: August 21, 2018
Omer R. Koseoglu, Adnan Al-Hajji, and Gordon Jamieson Yun Chang
Characterizing Petroleum Product Contamination Using Methods and Apparatus for Collecting and Preserving Core
Fluorescence Signal Samples from a Reservoir
Granted Patent: U.S. Patent 10,048,205, Grant Date: August 14, 2018 Granted Patent: U.S. Patent 10,053,938, Grant Date: August 21, 2018
Ezzat M. Hegazi, Vincent Cunningham, Christoph Stamm, and Anuj Gupta, Daniel T. Georgi, and Katherine L. Hull
Christof Brunner
System and Method for Condensate Blockage Removal with
Triaxial NMR Test Instrument Ceramic Material and Microwaves
Granted Patent: U.S. Patent 10,048,336, Grant Date: August 14, 2018 Granted Patent: U.S. Patent 10,053,959, Grant Date: August 21, 2018
Mustafa Hakimuddin Muhammad Ayub, Sameeh I. Batarseh, and Nabeel S. Habib
Magnetic Induction-based Localization for Wireless Computer Implemented Methods for Reservoir Simulation
Sensor Networks in Underground Oil Reservoirs with Automated Well Completions and Reservoir Grid Data
Granted Patent: U.S. Patent 10,048,400, Grant Date: August 14, 2018 Quality Assurance
Howard K. Schmidt, Ian F. Akyildiz, Shih-Chun Lin, and Abdullah A. Granted Patent: U.S. Patent 10,054,712, Grant Date: August 21, 2018
Shehri Mohammed S. Al-Nuaim, Omar A. Al-Nahdi, Tareq Al-Zahrani,
Khalid Al-Alwan, and Muath Al-Mulla
Predicting and Modeling Changes in Capillary Pressure and
Relative Permeabilities in a Porous Medium due to Mineral Field Deployable Docking Station for Mobile Robots
Precipitation and Dissolution Granted Patent: U.S. Patent 10,054,950, Grant Date: August 21, 2018
Granted Patent: U.S. Patent 10,049,172, Grant Date: August 14, 2018 Pablo Carrasco Zanini, Ali H. Outa, Fadl H. Abdel Latif, Brian J.
Shuo Zhang and Hui-Hai Liu Parrott, Sahejad Patel, Hassane Trigul, Ayman M. Amer, and Ali
Shehri
Floor Mat System and Associated, Computer Medium
and Computer Implemented Methods for Monitoring and Three-Dimensional Fluid Micromodels
Improving Health and Productivity of Employees Granted Patent: U.S. Patent 10,055,884, Grant Date: August 21, 2018
Granted Patent: U.S. Patent 10,052,023, Grant Date: August 21, 2018 Ali Alkhatib, Amar Alshehri, and Ming Han
Samantha J. Horseman
Non-Catalytic Hydrogen Generation Process for Delivery
Dual Catalyst System for Propylene Production to a Hydrodesulfurization Unit and a Solid Oxide Fuel Cell
Granted Patent: U.S. Patent 10,052,618, Grant Date: August 21, 2018
System Combination for Auxiliary Power Unit Application
Granted Patent: U.S. Patent 10,056,631, Grant Date: August 21, 2018
Sulaiman S. Al-Khattaf, Arudra Palani, Tazul I. Bhuiyan, Mohammad
N. Akhtar, Abdullah M. Aitani, Mohammed A. Al-Yami, and Sohel Thang V. Pham, Hasan Imran, and Mohamed Daoudi
Shaikh
Enhanced Electrochemical Oxidation of Carbonaceous Deposits
Process for Recovery of Light Alkyl Mono-Aromatic in Liquid Hydrocarbon Fueled Solid Oxide Fuel Cells
Compounds from Heavy Alkyl Aromatic and Alkyl-Bridged Granted Patent: U.S. Patent 10,056,635, Grant Date: August 21, 2018
non-Condensed Alkyl Aromatic Compounds
Stamatios Souentie and Ahmad Hammad
Granted Patent: U.S. Patent 10,053,401, Grant Date: August 21, 2018
Bruce R. Beadle, Vinod Ramaseshan, Rakan S. Bilaus, Omer R.
Koseoglu, and Robert P. Hodgkins
Granted Patent: U.S. Patent 10,060,899, Grant Date: August 28, 2018 Ahmad D. Hammad and Stamatios Souentie
Hydrocracking Catalyst for Hydrocarbon Oil, Method Multilateral Well Drilled with Underbalanced Coiled Tubing
for Producing Hydrocracking Catalyst, and Method for and Stimulated with Exothermic Reactants
Hydrocracking Hydrocarbon Oil with Hydrocracking Catalyst Granted Patent: U.S. Patent 10,087,736, Grant Date: October 2, 2018
Granted Patent: U.S. Patent 10,081,009, Grant Date: September 25, Abdulrahman A. Al-Mulhem
2018
Omer R. Koseoglu, Adnan Al-Hajji, Ali M. Al-Somali, Ali H. Flow Data Acquisition and Telemetry Processing System
Al-Abdulal, Mishaal Al-Thukair, Masaru Ushio, Ryuzo Kuroda,
Takashi Kameoka, Kouji Nakano, and Yuichi Takamori Granted Patent: U.S. Patent 10,088,347, Grant Date: October 2, 2018
Michael J. Black, Mohamed N. Noui-Mehidi, and Talha J. Ahmad
Modification of Bentonite Properties for Drilling Fluids
Granted Patent: U.S. Patent 10,081,751, Grant Date: September 25, Combined Water Cut and Salinity Meter
2018 Granted Patent: U.S. Patent 10,088,442, Grant Date: October 2, 2018
Mansour A. Al-Shafei, Akram A. Alfliow, Awadh M. Al-Mofleh, Jamal Michael J. Black and Mohamed N. Noui-Mehidi
M. Al-Aamri, Syed R.A. Zaidi, and Amer A. Al-Tuwailib
Granted Patent: U.S. Patent 10,081,756, Grant Date: September 25, Kamarul A. Amminudin
2018
B. Raghava Reddy and Matthew Hilfiger Separation Unit for Microbial and Scale Treatment
Granted Patent: U.S. Patent 10,092,860, Grant Date: October 9, 2018
Process for Oxidative Desulfurization and Sulfone Disposal Faisal Alabbas and Anthony Kakpovbia
Using Solvent Deasphalting
Granted Patent: U.S. Patent 10,081,770, Grant Date: September 25, Auto Thermal Reforming (ATR) Catalytic Structures
2018 Granted Patent: U.S. Patent 10,093,542, Grant Date: October 9, 2018
Abdennour Bourane, Omer R. Koseoglu, and Stephane C. Kressmann Jorge N. Beltramini, Moses O. Adebajo, Joao Carlos Diniz Da Costa,
Gao Qing Lu, Thang V. Pham, and Sai P. Katikaneni
Compositions of and Methods for Making Stable
Carbonaceous Nanomaterials Sulfur Asphalt in Roofing, Damp Proofing and Water Proofing
Granted Patent: U.S. Patent 10,082,016, Grant Date: September 25, Granted Patent: U.S. Patent 10,093,803, Grant Date: October 9, 2018
2018
Mohammed H. Al-Mehthel, Ibnelwaleed A. Hussein, Hamad I.
Carlos A. Zuniga, John B. Goods, Jason R. Cox, and Timothy M. Al-Abdulwahhab, and Saleh H. Al-Idi
Swager
Pulsed Hydraulic Fracturing with Nanosilica Carrier Fluid Carbon-based Fluorescent Tracers as Oil Reservoir
Nano-Agents
Granted Patent: U.S. Patent 10,113,406, Grant Date: October 30,
2018 Granted Patent: U.S. Patent 10,119,072, Grant Date: November 6,
2018
Noor O. Baqader, Ahmed M. Gomaa, Rajendra A. Kalgaonkar, Jin
Huang, Khalid R. Noaimi, and Ghaithan A. Al-Muntasheri Mazen Y. Kanj, Mohammad H. Rashid, and Emmanuel P. Giannelis
Determining Spotting Fluid Properties Supercritical Reactor Systems and Processes for Petroleum
Granted Patent: U.S. Patent 10,113,422, Grant Date: October 30, Upgrading
2018 Granted Patent: U.S. Patent 10,119,081, Grant Date: November 6,
Md. Amanullah and Turki T. Alsubaie 2018
Ki-Hyouk Choi, Abdullah T. Alabdulhadi, and Mohammed A.
Alabdullah
Organic Rankine Cycle-based Conversion of Gas Processing
Plant Waste Heat into Power
Measuring behind Casing Hydraulic Conductivity between
Granted Patent: U.S. Patent 10,113,448, Grant Date: October 30,
2018 Reservoir Layers
Mahmoud B. Noureldin and Akram H. Kamel Granted Patent: U.S. Patent 10,119,396, Grant Date: November 6,
2018
Noor M. Anisur Rahman
Systems for Recovery and Re-Use of Waste Energy in
Hydrocracking-based Configuration for Integrated Crude Oil
Refining and Aromatics Complex Variable Speed Pipeline Pig with Internal Flow Cavity
Granted Patent: U.S. Patent 10,113,805, Grant Date: October 30, Granted Patent: U.S. Patent 10,119,647, Grant Date: November 6,
2018 2018
Mahmoud B. Noureldin and Hani M. Al-Saed Mohamed A. Soliman
Methods and Compositions for in Situ Polymerization Reaction Sequential Fully Implicit Well Modeling of Transmissibility
to Improve Shale Inhibition for Reservoir Simulation
Granted Patent: U.S. Patent 10,125,301, Grant Date: November 13, Granted Patent: U.S. Patent 10,126,465, Grant Date: November 13,
2018 2018
Abeer M. Al-Olayan Ali H. Dogru
Filter Cake Removal Composition for Drilling Fluids and Attachment Mechanisms for Stabilization of Subsea Vehicles
Method of Use Thereof
Granted Patent: U.S. Patent 10,131,057, Grant Date: November 20,
Granted Patent: U.S. Patent 10,125,305, Grant Date: November 13, 2018
2018
Fadl H. Abdel Latif, Ali Outa, Sahejad Patel, Hassane Trigui,
Abdullah M. Al Moajil and Hisham A. Nasr-El-Din Abdullah Arab, Ammar Al Nahwi, and Ihsan Al-Taie
Stabilization of Petroleum Surfactants for Enhancing Oil N-Hydroxyalkylated Polyamines, Methods of Making
Recovery N-Hydroxyalkylated Polyamines, and Fluids Containing an
Granted Patent: U.S. Patent 10,125,307, Grant Date: November 13, N-Hydroxyalkylated Polyamine
2018 Granted Patent: U.S. Patent 10,131,622, Grant Date: November 20,
Yun Chang 2018
Matthew Hilfiger and B. Raghava Reddy
Process for Producing High Quality Coke in Delayed Coker
Utilizing Mixed Solvent Deasphalting Method for Preventing Formation of Water-Oil Emulsions
Granted Patent: U.S. Patent 10,125,318, Grant Date: November 13, Using Additives
2018 Granted Patent: U.S. Patent 10,131,830, Grant Date: November 20,
Omer R. Koseoglu 2018
Abduallah A. Al-Ghamdi, Aziz Fihri, Ihsan Al-Taie, Remi Mahfouz,
Integrated Process to Produce Asphalt and Desulfurized Oil Enrico Bovero, Mohammed Shahrani, and Haitham Aljahani
Sensor for Measuring the Electromagnetic Fields on Land and Loss Circulation Compositions Having Portland Cement Clinker
Underwater
Granted Patent: U.S. Patent 10,144,859, Grant Date: December 4,
Granted Patent: U.S. Patent 10,132,952, Grant Date: November 20, 2018
2018
B. Raghava Reddy
Alberto F. Marsala and Andrew Hibbs
Loss Circulation Compositions Comprising Portland Cement
Field Deployable Docking Station for Mobile Robots Clinker, a Suspending Medium and a High Aspect Ratio
Granted Patent: U.S. Patent 10,133,277, Grant Date: November 20, Material
2018 Granted Patent: U.S. Patent 10,144,860, Grant Date: December 4,
Pablo Carrasco Zanini, Ali H. Outa, Fadl H. Abdel Latif, Brian J. 2018
Parrott, Sahejad Patel, Hassane Trigul, Ayman M. Amer, and Ali B. Raghava Reddy
Shehri
Granted Patent: U.S. Patent 10,138,369, Grant Date: November 27, Rommel E. Arias Urbina
2018
Jay J. Farmer Measuring Spatial Wettability of a Porous Material Surface by
Nuclear Magnetic Resonance Gas Isotherm Technique
Granted Patent: U.S. Patent 10,145,774, Grant Date: December 4,
2018
Hyung T. Kwak and Ahmad M. Al Harbi
Settable, Form-Filling Loss Circulation Control Compositions Downhole Self-Isolating Wellbore Drilling Systems
Comprising in Situ Foamed Non-Hydraulic Sorel Cement Granted Patent: U.S. Patent 10,156,100, Grant Date: December 18,
Systems and Method of Use 2018
Granted Patent: U.S. Patent 10,150,905, Grant Date: December 11, Shaohua Zhou
2018
B. Raghava Reddy
Novel Method to Create Connectivity between Wellbore and
Subterranean Formation
Triggering Exothermic Reaction Using Microwave Granted Patent: U.S. Patent 10,156,129, Grant Date: December 18,
Granted Patent: U.S. Patent 10,151,186, Grant Date: December 11, 2018
2018 Fakuen F. Chang
Ayman R. Al-Nakhli
Systems and Methods for Wirelessly Monitoring Well
Location Sensor for a Rigless Deployed ESP System Conditions
Granted Patent: U.S. Patent 10,151,194, Grant Date: December 11, Granted Patent: U.S. Patent 10,156,136, Grant Date: December 18,
2018 2018
Brian A. Roth and Jinjiang Xiao Chinthaka P. Gooneratne, Bodong Li, and Shaohua Zhou
Nano-Level Evaluation of Kerogen-Rich Reservoir Rock Methodology to Quantify Reservoir Mineral of Chert
Granted Patent: U.S. Patent 10,151,714, Grant Date: December 11, Granted Patent: U.S. Patent 10,156,137, Grant Date: December 18,
2018 2018
Katherine L. Hull, Younane N. Abousleiman, and Sebastian Csutak Anas M. Al-Marzoug
Nano-Level Evaluation of Anisotropic Mechanical Properties of A Simple Method of Measuring the Connectivity between
Source Shale Different Pore Types in Porous Media by Using Low-Field NMR
Granted Patent: U.S. Patent 10,151,715, Grant Date: December 11, and Fast Field Cycling NMR Technique
2018 Granted Patent: U.S. Patent 10,156,531, Grant Date: December 18,
Younane N. Abousleiman and Katherine L. Hull 2018
Hyung T. Kwak, Ali A. Yousif, and Salah H. Saleh
Magnetic Induction-based Localization for Wireless Sensor
Networks in Underground Oil Reservoirs Method of Monitoring Fluids in Subsurface Reservoirs Using
Granted Patent: U.S. Patent 10,151,851, Grant Date: December 11, Nanoparticles and Induced Polarization Effect
2018 Granted Patent: U.S. Patent 10,156,654, Grant Date: December 18,
Howard K. Schmidt, Ian F. Akyildiz, Shih-Chun Lin, and Abdullah A. 2018
Shehri Alberto F. Marsala, Michael S. Zhdanov, and Vladimir Burtman
Sequential Fully Implicit Well Modeling of Transmissibility for System and Method for the Spectroscopic Detection of Oil
Reservoir Simulation Field Chemicals and Tracer Materials
Granted Patent: U.S. Patent 10,151,855, Grant Date: December 11, Granted Patent: U.S. Patent 10,156,658, Grant Date: December 18,
2018 2018
Ali H. Dogru Shannon L. Eichmann, Sehoon Chang, and Wei Wang
Novel Modular Electrochemical Cell and Stack Design Oil Swellable, Desolvated Polymer Gels and Methods of Using
Granted Patent: U.S. Patent 10,153,497, Grant Date: December 11, the Same for Preventing Loss of Non-Aqueous Wellbore Fluids
2018 to the Subterranean Formation
Ahmad D. Hammad, Stamatios Souentie, and Issam T. Amr Granted Patent: U.S. Patent 10,160,901, Grant Date: December 25,
2018
New Olefin Hydration Process Using Oscillatory Baffled B. Raghava Reddy
Reactor
Granted Patent: U.S. Patent 10,155,707, Grant Date: December 18, Maleic Anhydride Polymers and Methods of Treating
2018 Subterranean Formations
Abeer Arjah, Kareemuddin Shaik, and Wei Xu Granted Patent: U.S. Patent 10,160,902, Grant Date: December 25,
2018
B. Raghava Reddy
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Shale Gas Reservoir Development Strategies Using Complex Well Architectures Operating under Fixed Plateau
Rate Conditions
Dr. Mari H. Alqahtani, Prof. Turgay Ertekin, and Sultan M. Almalki
ABSTRACT
In this study, artificial neural networks (ANN) were used to develop a shale gas reservoir expert system. The developed expert
system provides solutions for complex wells instead of the typical massively hydraulically fractured horizontal wells (MHFHWs).
Holistic Evaluation of Water Cut in High GOR Wells for Better Production Management
Mohammad S. Al-Kadem, Dr. Dhafer A. Al-Shehri, Dr. Mohamed Mahmoud, and Dr. Rahul N. Gajbhiye
ABSTRACT
Water cut measurement becomes essential in fields where there is significant water production, especially when combined with
gas production, making the measurement of all three phases difficult. In other words, water cut measured values are affected by
the presence of gas near the surface. Therefore, the objective of this study is to estimate the water cut in high gas-oil ratio (GOR)
wells with values greater than 2,000 standard cubic ft/stock tank barrel (scf/stb)1.
Introduction of Real-Time Flow Measurements Opens New Paths to Overcome Challenges Encountered during the
Acid Stimulation of Extended Reach Wells
Laurie S. Duthie, Hussain A. Al-Saiood, Hamad M. Almarri, and Danish Ahmed
ABSTRACT
Challenges related to matrix acid stimulation and fluid placement in extended reach horizontal wells are usually exaggerated,
and demand a constant flow of innovation. The optimization of real-time fluid placement, increasing the reservoir contact and
establishing uniform fluid distribution for better production/injection across the open hole interval, is one area that can benefit
from these new innovations.
Estimating Transport Properties of Carbonate and Sandstone Rock Samples of Different Bedding Orientations:
Digital Rock Physics and Laboratory Measurements
Abrar A. Alabbad and Dr. Jack Dvorkin
ABSTRACT
Using coarse resolution digital images to estimate the effective transport properties of a rock provides us with a large field of
view, and a better representation of the rock’s textural heterogeneity. In this article, a digital rock physics (DRP) workflow
was developed to estimate a rock’s porosity, permeability, and electrical resistivity, using the bulk density, ρb, and photoelectric
factor, Pf , of the 3D data of nine core plugs that are comprised of sandstone. At each voxel, grain density, ρg, was estimated by
partitioning the sample between two minerals, and as such, porosity, ϕ, was calculated.