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Ahmad I 2015
Ahmad I 2015
PII: S1875-5100(15)30189-X
DOI: 10.1016/j.jngse.2015.09.056
Reference: JNGSE 1038
Please cite this article as: Ahmadi, M.A., Galedarzadeh, M., Shadizadeh, S.R., Colloidal Gas Aphron
Drilling Fluid Properties Generated by Natural Surfactants: Experimental Investigation, Journal of Natural
Gas Science & Engineering (2015), doi: 10.1016/j.jngse.2015.09.056.
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Colloidal Gas Aphron Drilling Fluid Properties Generated by
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Petroleum University of Technology, Ahwaz, Iran
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2)
Department of Petroleum Engineering, Abadan Faculty of Petroleum Engineering,
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*Corresponding Author: Department of Petroleum Engineering, Ahwaz Faculty of Petroleum
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Engineering, Petroleum University of Technology, Ahwaz, Iran. TEL: +98-912-6364936.
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Email: ahmadi6776@yahoo.com
Abstract
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Colloidal gas aphron (CGA) fluids are special types of fluids containing micro-bubbles with
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sizes between 10 to 100 microns which are created by mixing an aphronizer surfactant in a
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polymeric solution at high speed. Recently, CGA fluids have been successfully employed as
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drilling fluid in petroleum upstream. CGA based drilling fluid properties like stability and
a result, selection of an appropriate surface active agent plays a vital role for generating
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micro-bubbles with the favorable properties. The main objective of the present paper is to
evaluate the potential of new natural surfactants as aphronizer in CGA-based drilling fluids.
In this regard, two new natural surfactants which derived from roots of Seidlitzia Rosmarinus
and leaves of Henna plant are employed for preparing aphron-based fluids. Physico-chemical
properties of the aphronized fluids prepared from these surfactants were investigated by
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characterizations and stability tests. Moreover, the effects of polymer and surfactant
concentrations were studied systematically. Based on the experimental results obtained from
this work, the two aforementioned natural surfactants are appropriate for generating CGA
based drilling fluid while they have no environmental impacts, and have very low cost in
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Keywords: Natural Surfactant; Aphron Based Mud; Drilling; Stability; Drilling Fluid
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1. Introduction
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The majorities of known reservoirs in the world has reached their mature state and are
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classified as depleted. The problems related to drilling of these reservoirs make further
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development uneconomical. Uncontrollable fluid loss and the need for injection of lost
circulation materials (LCM) or in worst scenarios the injection of cement in the formation,
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imposes several mechanical and chemical damages to the near wellbore formation.
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Consequently, these damages reduce the productivity and productive interval of the drilled
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To minimize such problems the operators have shifted from conventional overbalance
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performance by minimizing drilling fluid invasion into the formation during drilling
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operation. However, there are many problems related to UBD including high equipment and
services costs, the unavailability of the technology in some areas, borehole instability, safety
concerns - especially in case of presence of hazardous gases such as H2S, etc. (Brookey et.
al., 2003;White et. al., 2003). Occasional overbalance moments during certain operations in
UBD can cause dramatic formation damages due to lack of filter cake on the borehole wall.
Such problems have limited the application of this technique in many areas.
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The need for a drilling fluid which reduces mud losses and formation damage and
simultaneously guarantees borehole stability and low cost, led to the introduction of aphron
based drilling fluids. The concept of colloidal gas aphron (CGA) fluids was first introduced
by Sebba in 1971 (Sebba, 1971). Later in 1987, he described its properties and predicted its
possible uses (Sebba, 1987). It was Brookey who first introduced the use of these novel fluids
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in drilling industry (Brookey, 1998). After the first successful application, CGA fluids were
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used for drilling depleted reservoirs in many fields around the world (Kinchen et. al., 2001;
Ivan et. al., 2001; Oyatomari et. al., 2002; Montilva et. al., 2002; Gregoire et. al., 2005;
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MacPhail et. al., 2008). For example, aphron fluid was used for drilling both the normal and
subnormal pore-pressure sections in Lake Maracaibo – after the failure of UBD system- and
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successfully reduced fluid loss and improved borehole stability. The application of aphron
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fluid in this field significantly reduced drilling operation time, saved one to two casing string
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per well, and enhancing well productivity and consequently improved oil recovery (Ramirez
Aphrons are bubbles, usually 10 to 100 microns in diameter and are generally composed of a
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gaseous core and a thin aqueous protective shell. In aqueous colloidal gas aphrons the shell is
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composed of an inner layer and outer surfactant bilayer. The inner layer contains surfactants
at the boundaries which are hydrophilic inward and hydrophobic outward. In order to be
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dispersed in water, the outer bilayer is hydrophilic outward (Sebba, 1987; Bjorndalen and
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Kuru, 2008).
The stability of aphron depends on the properties of viscous shell. The shell has to possess a
minimum thickness (Clunie et. al., 1967) and viscosity (Sebba, 1987; Scriven and
Sternling,1960). Aphron stability is determined by the rate of mass transfer between the
viscous water shell and the bulk phase. This mass transfer is known as the Marangoni effect
which is inversely proportional to the viscosity of protective shell (Sebba, 1987; Scriven and
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Sternling, 1960). Therefore polymers are added to the fluid in order to increase its viscosity
Another critical property which aphron fluids should possess, to guarantee their stability in
higher pressures, is low diffusivity of their films. At high pressures the solubility of air in
water increases. For conventional bubbles most of air molecules will diffuse and dissolve in
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water phase and consequently the bubbles disappeared in water. This diffusion is a very rapid
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process for conventional bubbles (Bredwell and Worden) ; however, aphron bubble will
remain stable for extended periods of time even at very high pressures owing to the viscous
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shell surrounding the gas core has a very low diffusivity that entrap the gas molecules (Ivan
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et. al., 2002). CGA fluids can tolerate very high pressures in the order of 4000 psi (Growcock
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et. al., 2007).
Aphron drilling fluid has the ability to reduce fluid loss in fractured and depleted formations.
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Aphrons are compressed when they are pumped down-hole. As a result, energy is stored in
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them and when a depleted formation is encountered, this energy is released and aphron
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expands until it reaches equilibrium with surrounding formation pressure (Ivan et. al., 2002).
On the other hand, the base fluid has a very high Low Shear-Rate Viscosity (LSRV)
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(Growcock et. al., 2004). Therefore when fluid enters the formation (a low-shear-rate region),
the viscosity builds rapidly. The expansion of aphrons and the increase in viscosity, both
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result in creation of a solid-free bridge. The solid-free bridge prevents further invasion of
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drilling fluid into the formation. Experience has shown that this bridge is easily removed by
back flowing the reservoir fluid, and there is no need for work-over operations at the end of
One advantage of aphrons over typical foams used in UBD is that they are easily created with
typical mud mixing equipment. Consequently, using aphrons eliminates the costs related to
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compressors and high-pressure equipment employed in foam drilling operation (White et. al.,
2003). Besides, unlike aerated muds, aphron fluids do not corrode drill string and other
drilling equipment, because most of air in the system is trapped in aphron shell (Bjorndalen
Recently, Ahmadi and colleagues investigated the use of the natural surfactants in oil
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recovery and wettability alteration goals in sandstone and carbonate reservoirs (Ahmadi and
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Shadizadeh, 2012; 2013a; 2013b; 2013c; 2014; Ahmadi et Al., 2014). In this study the use of
natural surfactants derived from leaves of Henna and roots of Seidlitzia Rosmarinus for
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employing in colloidal gas aphron (CGA) drilling fluids were investigated. The rheology and
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filtration loss properties of the aphronized fluids were studied systematically and the effects
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of surfactant and polymer concentrations were carried out.
The introduced surfactants have very low price relative to the commonly used surfactants in
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petroleum industry. They can be obtained around 1.5−2.0 US$/kg in Middle Eastern
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countries such as Iran and Egypt. They are also biodegradable and therefore more
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2. Material
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Two different types of natural surfactants which are extracted from roots of Seidlitzia
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Rosmarinus and leaves of Henna trees were used in this study. More details are illustrated
salt marshes and also in saline soils (Breckle, 1986; Hedge et al., 1997). The Seidlitzia genus
belongs to Chenopodiaceae family (Hedge et al., 1997). This species is named Seidlitzia
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Rosmarinus in honor of a botanist named Seidlitz (Sabeti, 1994). Application of natural
surfactant derived from roots of Seidlitzia Rosmarinus was firstly introduced by Deymeh et al.
2.2. Henna
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Henna (Lawsonia inermis, also known as hina, the henna tree, the mignonette tree, and the
Egyptian privet) (Bailey, 1976) is a flowering plant and the sole species of the Lawsonia
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genus (website). The Henna surfactant has been extracted from leaves of the Lawsonia
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inermis plant by implementing spray drier apparatus. The implication of Henna extract in
petroleum up-streams was firstly introduced by Ostovari et al., (2009) for corrosion inhibition
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goals. In addition, Abdolahi and Shadizadeh investigated the application of henna extract on
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acidizing of sandstone reservoirs (Abdolahi and Shadizadeh, 2012; 2013).
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3. Experimental
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The experimental procedures of this work was followed according to the below steps: 1)
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The base fluid was prepared by addition of different amounts of Xanthan Gum (XG)
biopolymer (1.5gr, 1.75gr, and 2gr) to de-ionized water. 350 cc (one laboratory barrel) of
distilled water was agitated and XG was added slowly to prevent the formation of local
agglomerates. The aforementioned solution was agitated for 20 minutes at a speed of 10000
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rpm. In this process some air bubble was trapped in the fluid and reduced the density to 8.2
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Aphronized fluid was prepared by adding the natural surfactants to the base fluid at different
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concentrations, and agitating the fluid with a disk type stirrer. The stirrer was placed just
below the surface level of base fluid and the rotation speed was set at 10000rpm for 2
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minutes. The position of disk type rotator was very important in proper generation of aphron
bubbles. The quantity of the aphrons generated significantly reduced by immersing the
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rotator too deep in the solution.
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The main mechanism of formation damage reduction in CGA fluids is the plugging of
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formation pores by aphrons. Therefore the size of aphrons is very important in the
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performance of CGA fluids, and has to be designed according to the pore size distribution of
formation rock.
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To determine the aphron size distribution, immediately after the preparation of aphronized
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fluid, a small sample of fluid was taken for imaging and size determination. The sample was
placed on an optical microscope which was connected to a digital video camera and the
camera was connected to a computer. For each sample 5-10 images was taken from different
parts of sample in order to obtain the average size and size distribution of aphrons. Computer
software was employed to determine the size of aphrons directly from the screen. Then the
average diameters of aphrons as well as size distribution and d10, d50, and d90 values were
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determined. d10, d50, and d90 are the values in which 10%, 50%, and 90%, respectively, of
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Rheological properties of aphronized fluid including plastic viscosity, yield point, gel
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strength, and apparent viscosity were measured by a Fann 35A Viscometer. Density of the
CGA fluid was determined either by a mud balance or by weighting a fixed volume of fluid.
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3.5. API fluid loss
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A Fann model 12BL filter press was employed for measuring API filtration loss. These
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experiments were conducted at 100 psig pressure and room temperature. The amount of
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The stability of aphrons is an important factor in final performance of CGA fluid. After
generating the CGA fluid, eventually because of buoyancy forces, aphron bubbles will
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separate from the bulk fluid and accumulate on upper level of fluid. The aphron bubbles will
break over time and consequently the volume of the fluid will shrink. To measure the stability
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of CGA fluids which created by the introduced natural surfactants, 100 ml of aphronized
fluid was poured in a test tube and the shrinkage of fluid volume was recorded after 72 hours.
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4. Results and discussion
The bubble diameter and size distribution of aphrons are very important factors which effect
on the pore bridging and blockage mechanism. Immediately after preparation the CGA fluid,
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a small sample of fluid was taken for imaging and size measurements. Figures 1 and 2
demonstrate two sample pictures taken from CGA fluids generated by surfactants extracted
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from Henna and Seidlitzia Rosmarinus, respectively. The viscous shells around the gas cores
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can be easily detected from these pictures.
Insert Figure 1
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Insert Figure 2
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The results of bubble size measurements are illustrated in Figures 3 to 7. The effect of
surfactant and polymer concentrations, surfactant type, and shear rate on size distribution,
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average aphron size and D10, D50 and D90 are depicted in these aforementioned Figures.
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Figures 3 and 4 illustrate the effect of surfactant concentration on aphron bubble size for
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Insert Figure 3
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Insert Figure 4
By increasing surfactant concentration, the average bubble size reduced for henna extract;
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however, it almost remains constant for Seidlitzia Rosmarinus extract. For both surfactants,
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d90 reduced by increasing surfactant concentration which proves the percentage of large
diameter bubbles reduced consequently. However, d10 and d50 remained fairly constant. By
increasing surfactant concentration, the average bubble diameter reduced from 100 μm to 78
μm for Henna extract, and from 85μm to 83µm for Seidlitzia Rosmarinus extract. This
approves the results published by Chaphalkar et al. (1993) who reported that an increase in
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The effect of polymer concentration on aphron bubble size for henna and Seidlitzia
Figures 5 and 6, the bubble size decreased significantly by increasing the polymer
concentration. This contradicts the results obtained by Bjorndalen and Kuru (2008), who
stated that an increase in polymer concentration has no significant effect on aphron bubble
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diameters.
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Insert Figure 5
Insert Figure 6
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Figure 7 shows the effect of shear rate on aphron bubble size. By increasing shear rate, d10
increased, d50 remained constant, and d90 decreased which shows that more intermediate
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bubbles are generated. These results can be confirmed by comparing the bubble size
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distributions at these two conditions.
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Insert Figure 7
Figures 8 to11 illustrate the bubble size distributions at different surfactant and polymer
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concentrations and different shear rates for Henna extract. As demonstrated in Figures 8 and
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9, by increasing surfactant concentration the number of medium and small diameter bubbles
concentration the percentage of small diameter bubbles significantly increased. The effect of
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shear rate on bubble size distribution is illustrated in Figures 10 and 11. It indicates that an
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increase in shear rate shifts the histogram to the right and it means that larger diameter
Insert Figure 8
Insert Figure 9
Insert Figure 10
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Insert Figure 11
The effects of surfactant and polymer concentrations on bubble size distribution for Seidlitzia
Rosmarinus extracts are illustrated in Figures 12 to 14. The same trend was observed for this
surfactant as Henna extract. Similarly, by raising the surfactant concentrations the number of
medium and small diameter bubbles increased adequately. On the other hand, by increasing
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polymer concentration in the solution the portion of the small diameter bubbles increased.
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Insert Figure 12
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Insert Figure 13
Insert Figure 14
of a surfactant to generate aphron bubbles. The results of density measurements show that,
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the density of fluid reduced from 8.3 ppg (for the base fluid) to 6 ppg for addition of 4 lb/bbl
Seidlitzia Rosmarinus extract. Figure 15 depicts the effect of surfactant concentration on the
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density of CGA fluid for both Henna and Seidlitzia Rosmarinus surfactants. The density of
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CGA fluid reduced from 6.7 ppg to 6.4 ppg by raising concentration of surfactant derived
from Henna from 1 lb/bbl to 4 lb/bbl. Due to the density measurement observations, Seidlitzia
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Rosmarinus surfactant had a better performance in generating aphron bubbles and reduced
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the density from 6.6 ppg to 6 ppg for 1 lb/bbl and 4 lb/bbl of surfactant concentrations,
respectively.
It should be pointed out that the density measurements were taken under atmospheric
pressure condition. At higher pressures (for instance, in down-hole conditions) the aphrons
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Insert Figure 15
The effect of polymer concentration on density of CGA fluid is illustrated in Figure 16. It
indicates that, as the concentration of XG increases, the density of fluid increases too. By
increasing polymer concentration the viscosity of base fluid increased. Therefore, the volume
of air entrained (the quantity of aphrons) reduced, and consequently the density increased.
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Insert Figure 16
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4.3. Rheology
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The experimental results showing the effect of natural surfactants and polymer concentration
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on rheology of aphronized fluids are illustrated in Tables 1 to 4.
According to Tables 1 and 3, by increasing the surfactant content, the value of plastic
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viscosity, yield point and apparent viscosity gradually increased. However, the magnitude of
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these properties for the Seidlitzia Rosmarinus extract at the same conditions is greater than
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corresponding values for surfactant extracted from henna. By comparing these results with
the outcomes reported in Figure 15, it can be concluded that by increasing in the amount of
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aphrons (i.e. decrease in fluid density) the viscosity of CGA fluid increased. However, gel
Tables 2 and 4, show the effect of polymer concentration on rheological properties of CGA
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fluids. By increasing polymer concentration, at constant surfactant content, the value of all
rheological properties increased. By comparing these results with Tables 1 and 3, it can be
concluded that the viscosity of CGA fluid is highly depends on both surfactant and polymer
concentrations, but the gel strength is mainly depends on the polymer concentration.
Insert Table 1
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Insert Table 2
Insert Table 3
Insert Table 4
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4.4. API filtration loss
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The viscosity of aphronized fluid as well as the quantity and size of aphrons can effect on the
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amount of filtration loss. The results of API filtration tests are presented in Figures 17 and 18.
The aphronized fluids were able to reduce the API fluid loss and spurt loss in comparison
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with the base fluid. As illustrated in Figures 17 and 18, by increasing the surfactant
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concentration the API fluid loss reduced for Henna extract; however, it didn’t change
significantly for surfactant derived from Seidlitzia Rosmarinus. As depicted in Figure 2, the
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increase in concentration of the surfactant derived from Seidlitzia Rosmarinus had little effect
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on size and size distribution of aphrons. This can be a reason for little change in fluid loss of
Insert Figure 17
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Insert Figure 18
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This section describes the results obtained from stability tests for CGA fluids. No volume
shrinkage was observed for CGA fluid prepared from both surfactants after 24 hours. Figures
19 and 20 illustrate the status of CGA fluids created by henna and Seidlitzia Rosmarinus
extracts after 72 hours, respectively. As depicted in Figure 19, for surfactant derived from
henna, most of aphrons were separated from the bulk phase and accumulated on top of liquid
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phase. On the other hand, Seidlitzia Rosmarinus had a great stability and no shrinkage of
volume, or separation of aphron bubbles from the bulk phase was observed for this surfactant.
Insert Figure 19
Insert Figure 20
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Conclusions
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The ability of two natural surfactants to generate aphronized fluid was investigated
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scientifically. Surfactants extracted from Henna and Seidlitzia Rosmarinus were able to
generate CGA fluids like commonly used commercial surfactants in drilling industry. The
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effect of surfactant and polymer concentrations on physical and rheological properties of the
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aphronized fluids was thoroughly investigated. Generally by increasing surfactant or polymer
concentration reduces the density of aphronized fluid and this means that more aphron
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bubbles are generated. On the other hand, higher polymer concentrations resulted in higher
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fluid density. The rheological tests revealed that the viscosity of CGA fluid is highly
depended on both surfactant and polymer concentrations; however, the gel strength of CGA
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fluid is mainly depends on the polymer concentration. The aphronized fluids generated by
both natural surfactants were able to reduce filtration loss in comparison with the base fluid.
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Moreover, by increasing surfactant concentration the API fluid loss reduced for henna
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extract; however, it didn’t change significantly for surfactant derived from roots of Seidlitzia
Rosmarinus. Finally, stability tests revealed that CGA fluid prepared by Seidlitzia
Rosmarinus extract has higher stability than the one prepared by henna extract.
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Tables
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Table 1: The effect of surfactant concentration on rheological properties for henna surfactant
(prepared by using 1.75 lb/bbl XG solution)
surfactant concentration
properties 0 1 2 4
plastic viscosity 10 12 14 14
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yield point 27 33 31 34
apparent viscosity 23.5 28.5 29.5 31
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Gel strength 10sec 12 14 14 15
Gel strength 10min 16 17.5 18 18
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Table 2: The effect of polymer concentration on rheological properties for henna surfactant
(prepared by adding 1 lb/bbl surfactant to the base fluid)
polymer concentration
properties 1.5 1.75 2
plastic viscosity 10.5 12 15
yield point 25.5 33 34
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apparent viscosity 23.25 28.5 32
Gel strength 10sec 10 14 17
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Gel strength 10min 14 17.5 21
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Table 3: The effect of surfactant concentration on rheological properties for Seidlitzia
Rosmarinus extract (prepared by using 1.75 lb/bbl XG solution)
surfactant concentration
properties 0 1 2 4
plastic viscosity 10 12 17 18
yield point 27 31 35 37
PT
apparent viscosity 23.5 27.5 34.5 36.5
Gel strength 10sec 12 14 14 15
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Gel strength 10min 16 18 18 18
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polymer concentration
properties 1.5 1.75 2
RI
plastic viscosity 11 12 16
yeild point 29 31 34
SC
apparent viscosity 25.5 27.5 33
Gel strength 10sec 12 14 17
Gel strength 10min 15 18 21
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Figures
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Figure 1: Microscopic picture of aphronized fluid prepared from henna extract
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Figure 2: Microscopic picture of aphronized fluid prepared from Seidlitzia Rosmarinus
extract
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200
180
Aphron diameter (micrometer)
160
140
120
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80
60
RI
40
20
SC
0
1 2 4
Amount of surfactant (lb/bbl)
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d10 d50 d90 Avg.
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Figure 3: Effect of henna extract concentration on bubble size (at 1.75 lb/bbl of XG solution)
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200
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140
120
100
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80
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1 2 4
Amount of surfactant (lb/bbl)
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d10 d50 d90 Avg.
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Figure 4: Effect of Seidlitzia Rosmarinus extract concentrations on bubble size (at 1.75 lb/bbl
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of XG solution)
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250
150
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100
RI
50
SC
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1.5 1.75 2
Amount of polymer (lb/bbl)
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Figure 5: Effect of polymer concentration on bubble size (at 1 lb/bbl henna extract
concentration)
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160
140
Aphron diameter (micrometer)
120
100
80
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60
40
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20
SC
0
1.5 1.75 2
Amount of polymer (lb/bbl)
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d10 d50 d90 Avg.
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Figure 6: Effect of polymer concentration on bubble size (at 1 lb/bbl Seidlitzia Rosmarinus
extract concentration)
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160
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Aphron diameter (micrometer)
120
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d10
80
d50
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60 d90
Avg.
40
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20
SC
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10000 11000
Shear Rate (RPM)
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Figure 7: Effect of shear rate on bubble size (prepared by 1 lb/bbl henna extract and 2 lb/bbl
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xanthan gum).
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35
30
Percentage of all bubbles (%)
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15
10
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5
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30 50 70 90 110 130 150 170 190 200+
Aphron bubble size (microns)
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Figure 8: Bubble size distribution at 1.75lb/bbl XG and 1 lb/bbl henna extract
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35
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percentage of all bubbles (%)
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15
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Aphron bubble size (microns)
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Figure 9: Bubble size distribution at 1.75 lb/bbl XG and 4lb/bbl henna extract
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35
30
percentage of all bubbles (%)
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15
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10
SC
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Aphron bubble size (microns)
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Figure 10: Bubble size distribution at 2 lb/bbl XG and 1 lb/bbl henna extract
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25
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PT
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Aphron bubble size (microns)
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Figure 11: Bubble size distribution at 2 lb/bbl XG and 1 lb/bbl henna extract (at 11000 rpm)
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Aphron bubble size (microns)
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Figure 12: Bubble size distribution at 1.75 lb/bbl XG and 1 lb/bbl Seidlitzia Rosmarinus
extract concentration
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Aphron bubble size (microns)
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Figure 13: Bubble size distribution at 1.75 lb/bbl XG and 4 lb/bbl Seidlitzia Rosmarinus
extract concentration
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Aphron bubble size (microns)
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Figure 14: Bubble size distribution at 2 lb/bbl XG and 1 lb/bbl Seidlitzia Rosmarinus extract
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concentration
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9
8.5
7.5
weight (ppg)
6.5
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6
5.5
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4.5
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0 1 4 1 4
hena rozmari
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surfactant concentration (lb/bbl in 2lb/bbl XG solution)
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Figure 15: Effect of surfactant concentration on density of CGA fluid
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6.5
6
Weight (ppg)
5.5
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5
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1.5 2 1.5 2
hena rozmari
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Polymer concentration (lb/bbl with 1lb/bbl surfactant)
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Figure 16: Effect of XG concentration on density of CGA fluid
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Fluid loss (ml)
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Amount of surfactant (lb/bbl)
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API fluid loss (ml/30min) Spurt loss
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Figure 17: Effect of henna extract concentration on API fluid loss and spurt loss (for 2 lb/bbl
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Fluid loss (ml)
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Amount of surfactant (lb/bbl)
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API fluid loss (ml/30 min) Spurt loss
Figure 18: Effect of Seidlitzia Rosmarinus extracted surfactant on API fluid loss and spurt
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Research Highlights
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evaluated.
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• Stability of the natural surfactants have been evaluated for 72 hour.
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