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Article

Prevention of Barite Sag in Water-Based Drilling Fluids by A Urea-Based Additive for Drilling Deep Formations

by
Abdelmjeed Mohamed
1,
Saad Al-Afnan
1,
Salaheldin Elkatatny
1,* and
Ibnelwaleed Hussein
2
1
College of Petroleum Engineering and Geosciences, King Fahd University of Petroleum & Minerals, Dhahran 31261, Saudi Arabia
2
Gas Processing Center, College of Engineering, Qatar University, Doha 2713, Qatar
*
Author to whom correspondence should be addressed.
Sustainability 2020, 12(7), 2719; https://doi.org/10.3390/su12072719
Submission received: 13 February 2020 / Revised: 19 March 2020 / Accepted: 26 March 2020 / Published: 30 March 2020
(This article belongs to the Special Issue Sustainability in Oil, Gas and Energy Resources)

Abstract

:
Barite sag is a challenging phenomenon encountered in deep drilling with barite-weighted fluids and associated with fluid stability. It can take place in vertical and directional wells, whether in dynamic or static conditions. In this study, an anti-sagging urea-based additive was evaluated to enhance fluid stability and prevent solids sag in water-based fluids to be used in drilling, completion, and workover operations. A barite-weighted drilling fluid, with a density of 15 ppg, was used with the main drilling fluid additives. The ratio of the urea-based additive was varied in the range 0.25–3.0 vol.% of the total base fluid. The impact of this anti-sagging agent on the sag tendency was evaluated at 250 °F using vertical and inclined sag tests. The optimum concentration of the anti-sagging agent was determined for both vertical and inclined wells. The effect of the urea-additive on the drilling fluid rheology was investigated at low and high temperatures (80 °F and 250 °F). Furthermore, the impact of the urea-additive on the filtration performance of the drilling fluid was studied at 250 °F. Adding the urea-additive to the drilling fluid improved the stability of the drilling fluid, as indicated by a reduction in the sag factor. The optimum concentration of this additive was found to be 0.5–1.0 vol.% of the base fluid. This concentration was enough to prevent barite sag in both vertical and inclined conditions at 250 °F, with a sag factor of around 0.5. For the optimum concentration, the yield point and gel strength (after 10 s) were improved by around 50% and 45%, respectively, while both the plastic viscosity and gel strength (after 10 min) were maintained at the desired levels. Moreover, the anti-sagging agent has no impact on drilling fluid density, pH, or filtration performance.

1. Introduction

Drilling fluids are introduced to a formation to fulfill many functions, but mainly to control the formation pressure [1,2]. Overbalanced drilling is a common technique for well control, where the drilling fluid provides a hydrostatic pressure higher than the formation pressure. To achieve this function, the required fluid density is maintained by adding weighting materials to the drilling fluid. There are many weighting materials introduced to increase the drilling fluid density, such as barite, siderite, magnetite, iron oxides, ilmenite, hematite, and calcite [2,3,4,5,6,7,8,9,10]. Barite (BaSO4) is a common weighting material used to attain the desired density of drilling and completion fluids [2,11] because barite has a high density, low production cost, and less environmental impact [12,13]. However, the invasion of solid particles causes formation damage and reduces the permeability near the wellbore [14,15]. Another issue encountered with barite-weighted fluids is solids sag or barite sag.
Barite sag is a phenomenon that occurs when barite particles separate from the liquid phase and settle down, causing variations in fluid density. These variations may cause a loss of well control that could lead to severe kick [16,17]. Barite sag is a serious issue encountered in vertical and directional wells, but more commonly in directional wells. It can occur under either static conditions or dynamic conditions, particularly at low shear rates [16,18]. Several cases of barite sag have been encountered in drilling and completion operations [19]. For instance, a severe kick was detected during a well completion operation in the North Sea. In that operation, oil-based mud was used as a completion fluid. The kick resulted due to barite sag, with a significant contribution of well geometry to the solids sag issue [20]. However, the consequences of barite sag can be mitigated by maintaining the drilling fluid rheology, implementing sound strategies, and training rig personnel [19]. Using drilling fluid additives is the most effective solution to the problem of barite sag as it greatly enhances the drilling fluid rheology and stability, which are considered the main controlling factors of barite sag.
Many studies have been conducted to mitigate the solids sag phenomenon in both oil-based and water-based drilling fluids by adding drilling fluid additives and controlling the weighting material. Temple et al. [21] introduced a new method to enhance the stability of oil-based fluids without increasing the drilling fluid viscosity. Polyalkyl methacrylate, with low molecular weight, was added to the drilling fluid, while no copolymer such as vinylpyrrolidone was used. Davis et al. [22] introduced a new method to prevent solids sag in oil-based fluid by using a sag stability enhancer. The sag stability enhancer comprises polyethylene glycol (PEG) that has a molecular weight equal to or higher than 200 g/mol. Basfar et al. [23] and Elkatatny [24] evaluated a new copolymer to mitigate solids sag in oil-based mud at high temperatures, up to 350 °F. Just 1 lbm/bbl of the copolymer was enough to solve the barite sag issue in both vertical and inclined conditions. Boyou et al. [25] performed an experimental study on the use of nano-silica to improve the suspension capability of water-based fluids for directional well drilling applications. Different concentrations of nano-silica were used, and the experiments were conducted in a flow loop setup at different inclination angles. It was found that nano-silica increased the colloidal interaction with cuttings; therefore, the cuttings’ transport efficiency was significantly improved in all inclination angles.
Another technique for reducing barite sag is to modify the weighting material without adding a stability enhancer to the drilling fluid. Alabdullatif et al. [26] proposed a combination of manganese tetra oxide (Mn3O4) and barite as a weighting material in water-based kill fluid to mitigate the problem of barite sag. Adding Mn3O4 to the fluid formulation effectively enhanced the fluid stability and minimized the possibility of solids sag, particularly over a long time under static conditions. Mohamed et al. [13] investigated the impact of barite particle size reduction on the stability of water-based mud using the sag test and zeta potential measurements. It was concluded that decreasing the barite particle size to micronized size slightly enhances the drilling fluid stability, but it does not eliminate the sag issue. Basfar et al. [27] and Mohamed et al. [28] studied the effect of using a barite-ilmenite combined weighting material on the properties of water-based and oil-based drilling fluids. It was found that the combined weighting material greatly enhanced the rheological properties and the stability of the drilling fluid and prevented solids sag in both vertical and inclined conditions. However, using a combined weighting agent would add more cost and introduce another challenge to the drilling fluid operation, that is, the removal of composite filter cake, as the weighting material contributes greatly to filter cake formation, at 70–80 wt.% [29].
For successful operations, the rheology of the drilling fluid should be monitored and maintained throughout drilling operations by adding the proper drilling fluid additives such as viscosifiers, thinners, and stability enhancers. Most of the previous studies related to barite sag were conducted on oil-based fluids, and barite sag in water-based drilling fluids has received little attention. The previous studies focused on measuring the sag tendency and tried to correlate the results with the rheological and viscoelastic properties (see Table 1).
In this study, an anti-sagging additive is introduced as another solution to enhance fluid stability and eliminate solids sag in water-based drilling, completion, and workover fluids, without introducing a combined weighting material to the drilling fluid that would lead to a complex solids system, or adding high cost to the drilling operation, because very low concentrations of this additive are required. This additive is a modified urea solution and was originally used in water-based applications for anti-sag in other industries, such as coatings, lubricants, foundries, and detergent industries [30,31]. The extension of the application of this additive to water-based drilling fluids for deep wells is investigated. First, the materials used are described, and the experimental procedure and conditions to conduct this work are explained. Then, the results of this study are discussed, and lastly, the findings of this work are summarized.

2. Materials

The barite sample, obtained from a service company, was used as a weighting material for water-based drilling fluid. The elemental composition of the barite sample was obtained using the X-ray fluorescence technique, XRF. The barite sample mainly contains 82 wt.% barium, 12.6 wt.% sulfur, 1.99 wt.% silicon, and 1.33 wt.% iron, with small traces (<1 wt.%) of other elements, such as potassium, calcium, nickel, copper, and strontium (Table 2). The particle size distribution of this sample was measured using a particle size analyzer. The sample exhibited a normal distribution with a D10 of 4.5 µm, average particle size (D50) of 30 µm, D75 of 52 µm, and D90 of 79 µm (Figure 1). Defoamer (D-Air 4000L™) was added to the water to prevent the formation of foam. The defoamer comprises an amide of carboxylic acid, a polypropylene glycol, an ethoxylated and propoxylated fatty alcohol, an ethoxylated alcohol comprising from 3 carbons to 6 carbons, and a hydrophobic silica in an amount of up to about 3% by weight of the defoaming composition. Soda ash was used to maintain the concentration of calcium in the water. Xanthan gum polymer and bentonite were used as viscosifiers to improve the drilling fluid rheology. Starch and Polyanionic Cellulose Regular Viscosity (PAC-R) were used to control fluid loss. Clay stabilization was maintained by adding potassium chloride to the drilling fluid. Calcium carbonate was used as a bridging agent, and potassium hydroxide was used to control the pH of the drilling fluid [7].
The anti-sagging additive was added in different concentrations, 0.25–3 vol.% of the total base fluid, to improve the stability of the drilling fluid and prevent solid settlement. It was added right before the weighting material, barite, and mixed for 10 min. This additive works as an anti-sagging agent, and it is a solution of modified urea that mainly contains pentanoic acid, 5-(dimethylamino)-2-methyl-5-oxo-, methyl ester, and lithium chloride (Table 3). It was obtained from a service company, and it was originally used in coatings, lubricants, foundries, and detergent industries as an anti-sagging agent. It has a density of 1.11 g/cc and dynamic viscosity of 700 mPa.s at ambient temperature, with complete solubility in water.

3. Experimental Work

3.1. Fluid Preparation

A barite-weighted drilling fluid, 15 ppg, was prepared using the main drilling fluid additives. Drilling fluid additives were added individually and mixed for a specific time initially by adding viscosifiers (xanthan gum polymer and bentonite). The mixing started with 10,000 rpm rotational speed, then increased to 14,000 rpm and then to 17,000 rpm as the viscosity built up. Afterward, other additives were added to the drilling fluid following the fluid formulation used (Table 4). Following the same procedure, many fluid samples were prepared by adding different concentrations of the urea-additive to the drilling fluid formulation (0.25, 0.5, 1.0, 1.5, 2.0, and 3.0 vol.% of the total base fluid). The urea-additive was added right before adding the weighting material and mixed for 10 min.

3.2. Sag Tests

First, the sag test was conducted using the base drilling fluid at two different temperatures, 200 and 250 °F, to identify the temperature at which barite sag occurs. Then, the effect of the urea-additive on the sag tendency was evaluated at that temperature. The experimental setup consists of Teflon liner, aging cell, cell holder, and oven (Figure 2). First, the drilling fluid sample was agitated using the drilling fluid mixer for 10 min, and then poured in the cell. The fluid samples were pressurized with 500 psi using nitrogen and heated to 200/250 °F for 24 h under static conditions, vertical and inclined (45°). After 24 h, the cell was cooled and depressurized; then, a syringe was used to take a 10 cm3 sample from the top and the bottom fluid, and the density of those samples was measured. Then, the sag factor was obtained using Equation (1). Sag tests were repeated three times to ensure the accuracy of the measurements, and the presented data are the average of the measurements.
S a g   F a c t o r = ρ B o t t o m ρ B o t t o m + ρ T o p  
where ρBottom and ρTop are the density of the bottom and top fluid samples in ppg.
According to industry practices, the acceptable value of the sag factor is between 0.5 and 0.53, while a higher value indicates solids settlement [26,32].

3.3. Rheology Measurement

After preparing the drilling fluid, the drilling fluid density was measured, and the rheology measurements were conducted at low temperature (80 °F) and high temperature with high pressure (250 °F and 2000 psi) to study the effect of the urea-additive on the drilling fluid rheology in those conditions. The measured properties are yield point (YP), plastic viscosity (PV), and gel strength after 10 s and 10 min. Plastic viscosity and yield point are calculated by Equations (2) and (3) using the dial readings at 300 RPM (ϕ300) and 600 RPM (ϕ600), while the gel strength data were obtained from the direct dial reading at 3 RPM after 10 s, 10 min, and 30 min of static gel time.
P V = 600 300  
Y P = 300 P V  

3.4. HPHT Filtration Experiments

The filtration performance of the drilling fluid and the filter cake properties were evaluated by conducting a series of filtration experiments. The test was conducted at 250 °F and 300 psi differential pressure, using a 50-micron ceramic filter disc as a filtration medium. The high-pressure high-temperature (HPHT) filtration cell was heated to 250 °F under a pressure of 300 psi (Table 5). Afterward, the experiment was started, and the filtrate volume was measured with time. After 30 min, the experiment was stopped, the filter cake was weighted, and the thickness of the filter cake was measured.

4. Results and Discussions

4.1. Sag Tests

First, the drilling fluid density and the pH were measured for the drilling fluid samples. It was found that adding the anti-sagging additive at a concentration up to 3 vol.% of the total base fluid had no impact on drilling fluid density and pH. The density was around 15 ppg for all fluid samples, and the pH ranged between 9 and 10.
The sag performance of the base drilling fluid under vertical and inclined conditions was measured at two different temperatures, 200 and 250 °F. For the inclined sag test, the degree of inclination was set at 45° to simulate the worst scenario because the settling process is accelerated when the inclination is greater than 30° [33]. At 200 °F, the base drilling fluid exhibited a good sag performance in both cases, vertical and inclined, and the sag factor was within the safe range (0.5–0.53) with values of 0.51 and 0.52, respectively (Figure 3). In contrast, the base fluid showed a poor sag performance at 250 °F. The sag factor was higher than 0.53 for both inclined and vertical conditions; therefore, barite sag is highly anticipated.
Under vertical conditions, adding the anti-sagging additive to the drilling fluid formulation showed a significant improvement in the drilling fluid stability at 250 °F, the sag factor was within the acceptable range (0.5–0.53) for all the drilling fluid samples, and adding just 0.25 vol.% of the anti-sagging additive was adequate to prevent barite sag (Figure 4). Conversely, when the sag test was conducted under inclined conditions, 45°, Figure 5 shows that adding 0.25 vol.% of the anti-sagging additive reduced the sag factor from 0.63 to 0.54, and adding 0.5–1 vol.% was adequate to bring the sag factor into the safe zone (0.5–0.53); thus, barite sag is unlikely to occur under those conditions. The improvement in the sag tendency of the drilling fluid is because the urea-additive helped disperse the particles in the colloidal system and improved the suspension capability of the drilling fluid [34].

4.2. Rheological Analysis

The shear stress measured at room temperature (80 °F) was plotted versus the shear rate for all the drilling fluid samples (Figure 6). It was observed that the drilling fluid samples follow the Bingham plastic model. Increasing the concentration of the anti-sagging additive increased the shear stress values and shifted the consistency curve upward with almost a constant slope. This shift indicates a significant increase in yield point (intercept with the y-axis) without increasing the plastic viscosity (slope).
The effect of adding the urea-additive on the rheological properties was evaluated by measuring yield point, plastic viscosity, and gel strength at 10 s and 10 min. At room temperature, a significant increase in the yield point and gel strength values after 10 s was observed as the concentration increased (around 40%–50% for 0.5–1.0 vol.%), reflecting an enhancement in the drilling fluid’s ability to suspend solid particles (Figure 7). In contrast, the anti-sagging additive had no impact on plastic viscosity and gel strength values after 10 min. All the drilling fluid samples had a plastic viscosity of around 25 cP, and a gel strength (after 10 min) of around 45 lbf/100ft2. When YP/PV ratios were calculated for all drilling fluid samples (Figure 8), it was found that as the concentration of the anti-sagging agent increased, the YP/PV ratio increased, indicating a more stable drilling fluid, which confirms the sag test results.
The yield-stress characteristics affect many drilling fluid issues such as hole cleaning, barite sag, surge and swab pressures, and equivalent circulating density [35]. YP/PV was proposed as a tool to evaluate drilling fluid stability [36]. From the rheology measurements, as the concentration of the anti-sagging additive was increased, the YP/PV ratio increased, which reflects an enhancement in fluid stability and in the drilling fluid’s capability to suspend solid particles. However, adding high concentrations of the anti-sagging additive will require higher pumping pressure to start the drilling fluid circulation because of the high yield point and gel strength values [37]. Moreover, very high YP/PV ratios indicate mud coagulation and flocculation [36]. Since adding just 0.5–1 vol.% of the anti-sagging additive prevented barite sag in both vertical and inclined conditions, 0.5–1 vol.% can be considered as the optimum concentration of the anti-sagging additive. Adding more than this concentration would cause additional pressure losses because the yield point affects the pressure losses for Bingham plastic fluids. Moreover, increasing the concentration of the urea-additive would also increase the total cost of the drilling operations.
Furthermore, the drilling fluid rheology for the base fluid and with 0.5–1.0 vol.% of the anti-sagging additive was measured at 250 °F and 2000 psi. The measurements were performed to evaluate the performance of the urea-additive at high pressure and temperature. All samples showed similar behavior to that at room temperature with lower values of yield point, plastic viscosity, and gel strength because of the high-temperature effect (Figure 9; Figure 10). A huge drop, 76%, in the plastic viscosity of the base fluid was observed, while the anti-sagging additive significantly reduced that drop to around 50% and improved the plastic viscosity at the elevated temperature. The YP/PV ratio was within the acceptable range for all the drilling fluid samples (1.5 to 3), according to drilling operation practices. However, the increase in the YP/PV ratio of the base drilling fluid at high temperature compared with that at low temperature, from 1.13 to 2.4, can be attributed solely to the huge drop in the plastic viscosity. No enhancement in the yield point was observed, while adding the anti-sagging additive maintained the YP/PV ratio of the drilling fluid at high temperature with acceptable plastic viscosity and yield point values.

4.3. HPHT Filtration Experiments

Figure 11 compares the filtration performance curve of the base fluid, 0.5 vol.%, and 1 vol.% drilling fluid samples. It was found that the anti-sagging additive did not affect the filtration performance significantly, and the drilling fluid samples had similar filtration performances. The filtration experiments were conducted using a ceramic filter disc with uniform porosity and permeability to fairly compare the results and eliminate the effect of formation heterogeneity [38]. A difference of around 1.4 cm3 in the total volume of the fluid filtrate was observed, and the filter cake weight and thickness were almost the same (Figure 12). The filtration experiment results are summarized in Table 6.
The anti-sagging additive was proven to be effective in preventing barite sag in aqueous drilling fluids with the formulation used in this study. However, more research work is needed to determine the optimum concentration required for different drilling fluid formulations before use in field operations. Moreover, a lab study should be conducted to evaluate the performance of this additive at higher solids loading and salt concentrations and ultra-high temperatures.

4.4. Molecular Investigation of Fluid Loss Control Agents

Molecular simulation can be employed to shed some light on the performance of fluid loss control additives. These polymeric substances tend to accumulate on the surfaces of the wellbore, creating an impermeable layer to avoid further drilling fluid invasion. In the experimental part, starch and polyanionic cellulose were used for this purpose. The two polymers were recreated on a molecular platform, as shown in Figure 13. Polymer Consistent Force Field (PCFF+), which has the capability of capturing the properties of all the atoms present in the system, is used to define the intermolecular atom types and charges. Detailed assignments of bonding are given in the first part of the Appendix A. The molecular simulation was then carried out with the objective of forming a thin polymeric layer in typical reservoir conditions and then characterizing its porosity. The latter serves as an indicator of how well sealed the formed layer is.
Two thin layers of starch and PAC were formed in reservoir conditions of 250 °F and 3000 psi, as shown in Figure 14. The molecular simulation protocol consisted of initialization with a 9.5 cutoff value, followed by an constant particle number, volume and temperature (NVT) stage run for 250 ps and then a series of four NPT stages of 200, 200, 400, and 400 ps, respectively, performed using LAMPPS open source software assisted by the MedeA interface.
Then, a porosity estimation was carried out using He-pycnometry simulations through the Gibbs isotherm module of MedeA. Helium adsorption calculations are given in the Appendix A. The estimated porosity values were around 3% for both cases, indicating that the drilling fluid invasion is minimized when those polymers are employed.

5. Summary and Conclusions

Extensive experimental work was conducted to assess an anti-sagging additive and study its impact on the properties of barite-weighted drilling fluid and the barite sag tendency. Based on the results of this study, the following conclusions are drawn:
  • Adding 0.5–1.0 vol.% of the urea-additive to the base drilling fluid increased the yield point and gel strength after 10 s at 80 °F by around 40–50%. Moreover, the plastic viscosity and gel strength after 10 min remained almost constant. At 250 °F, a 76% drop in the plastic viscosity was observed for the base drilling fluid, while the urea-additive reduced that drop to around 50% and maintained the YP/PV ratio at that temperature.
  • Adding just 0.5–1.0 vol.% of the urea-additive was adequate to enhance the drilling fluid stability and prevent barite sag at 250 °F. The sag factor was around 0.51 under both vertical and inclined conditions.
  • The urea-additive had no impact on the density and the pH of the drilling fluid, while it had minimal effect on the filtration performance of the drilling fluids and the properties of the formed filter cake. The total fluid filtrate increased by around 1.4 cm3, while the filter cake properties were almost the same. However, fluid loss control agents such as starch and polyanionic cellulose can help in minimizing drilling fluid invasions. Molecular simulation of polymeric accumulations showed that a thin layer of low porosity is formed under typical reservoir conditions.
  • The developed formulation can be used to drill deep formations efficiently without the barite sag issue at a temperature up to 250 °F. Furthermore, the concentration of the urea-additive should be optimized for different fluid formulations before using it in real field applications. More research work is needed to evaluate the performance of this urea-additive at higher solids loading, high salt concentrations, and ultra-high temperature and pressure. An experimental study is also needed to evaluate the interaction of this additive with formation rocks and fluids and how this may affect the formation damage.

Author Contributions

Conceptualization, S.E.; Methodology, A.M., S.A.-A., and S.E.; Formal Analysis, A.M., S.E., and I.H.; Investigation, A.M., S.A.-A., and S.E.; Resources, S.E. and I.H.; Data Curation, A.M. and S.E.; Writing—Original Draft Preparation, A.M. and S.A.-A.; Writing—Review and Editing, A.M., S.A.-A., S.E., and I.H.; Visualization, A.M.; Supervision, S.E. and I.H.; Project Administration, S.E. All authors have read and agreed to the published version of the manuscript.

Funding

This research received no external funding.

Acknowledgments

The authors wish to acknowledge King Fahd University of Petroleum and Minerals (KFUPM) for allowing them to utilize various facilities in carrying out this research. Many thanks are due to the anonymous referees for their detailed and helpful comments.

Conflicts of Interest

The authors declare no conflict of interest.

Appendix A

i-
Forcefield assignments
Table A1. Starch.
Table A1. Starch.
Atom #NameElementAtomic NumberWycoff
Position
Wycoff
Equation
XYZFF Atom
Type
Charge
1C1C61ax,y,z0.1729910.3318750.762531c3−0.159
2C2C61ax,y,z0.2845690.3318750.762531c1oe0.107
3C3C61ax,y,z0.3221750.2400620.729939c43o0.107
4C4C61ax,y,z0.2905890.220670.623912c43o0.107
5C5C61ax,y,z0.3263740.2813480.545539c1oe0.107
6C6C61ax,y,z0.2889370.3748270.570667c1oe0.107
7O1O81ax,y,z0.322220.4010240.682899oc−0.32
8C7C61ax,y,z0.330470.4401720.490167c4o0.054
9O2O81ax,y,z0.2956680.5268540.513608oh−0.57
10O3O81ax,y,z0.4306050.2811290.546566oc−0.32
11C8C61ax,y,z0.4661560.3414410.468663coh0.267
12C9C61ax,y,z0.3901060.3755970.388848c43o0.107
13C10C61ax,y,z0.3171980.4261050.443868c43o0.107
14C11C61ax,y,z0.3547390.5025690.497479c1oe0.107
15C12C61ax,y,z0.4293640.4735450.581691c1oe0.107
16O4O81ax,y,z0.5113960.4204950.527721oc−0.32
17C13C61ax,y,z0.4726740.5549880.635556c2oe0.054
18O5O81ax,y,z0.5418820.5279290.713651oc−0.32
19C14C61ax,y,z0.5823440.6040080.76398coh0.267
20C15C61ax,y,z0.6860530.5653910.756915c43o0.107
21C16C61ax,y,z0.710630.5501350.647774c43o0.107
22C17C61ax,y,z0.7108060.6284850.583634c1oe0.107
23C18C61ax,y,z0.6080950.6696590.58369c1oe0.107
24O6O81ax,y,z0.5776830.6898140.698637oc−0.32
25C19C61ax,y,z0.609130.7551650.519422c4o0.054
26O7O81ax,y,z0.5137890.7932640.519565oh−0.57
27O8O81ax,y,z0.7791770.6903710.62576oc−0.32
28C20C61ax,y,z0.7793460.7682360.562002c3oe0.001
29O9O81ax,y,z0.8057730.5117770.643664oh−0.57
30O10O81ax,y,z0.6898930.4839140.813656oh−0.57
31O11O81ax,y,z0.4011980.5593760.422602oc−0.32
32C21C61ax,y,z0.4385110.635370.475895coh0.267
33C22C61ax,y,z0.5450240.6036230.468663c43o0.107
34C23C61ax,y,z0.5720160.5938980.359283c43o0.107
35C24C61ax,y,z0.5669070.6743120.29918c1oe0.107
36C25C61ax,y,z0.4612740.7089130.299555c1oe0.107
37O12O81ax,y,z0.4280210.7229540.414885oc−0.32
38C26C61ax,y,z0.4564660.7965240.239715c4o0.054
39O13O81ax,y,z0.3584240.8285220.240146oh−0.57
40O14O81ax,y,z0.6298240.7387540.345583oc−0.32
41C27C61ax,y,z0.6247370.8186710.285847c3oe0.001
42O15O81ax,y,z0.6699330.5617730.35487oh−0.57
43O16O81ax,y,z0.5544720.5206130.521278oh−0.57
44O17O81ax,y,z0.2460090.4545980.368657oh−0.57
45O18O81ax,y,z0.3449240.3025050.33691oh−0.57
46O19O81ax,y,z0.3237390.1341750.596919oh−0.57
47O20O81ax,y,z0.2842680.1751020.800825oh−0.57
48H1H11ax,y,z0.1468140.2835590.818172hc0.053
49H2H11ax,y,z0.1468140.3158690.684508hc0.053
50H3H11ax,y,z0.1468140.3961970.784912hc0.053
51H4H11ax,y,z0.3104670.3477280.840705hc0.053
52H5H11ax,y,z0.4006620.2393520.733125hc0.053
53H6H11ax,y,z0.2122780.2260870.623553hc0.053
54H7H11ax,y,z0.3008070.2616040.468519hc0.053
55H8H11ax,y,z0.2104940.375890.566526hc0.053
56H9H11ax,y,z0.3074870.4215970.411778hc0.053
57H10H11ax,y,z0.4089280.4394220.494222hc0.053
58H11H11ax,y,z0.2245440.5275310.509928ho0.41
59H12H11ax,y,z0.5179590.30540.421392hc0.053
60H13H11ax,y,z0.4255690.4167370.331hc0.053
61H14H11ax,y,z0.2870140.3836170.503795hc0.053
62H15H11ax,y,z0.295690.5373230.53516hc0.053
63H16H11ax,y,z0.3938350.4330890.640184hc0.053
64H17H11ax,y,z0.4152480.5921580.672863hc0.053
65H18H11ax,y,z0.5084380.5955310.577326hc0.053
66H19H11ax,y,z0.5500380.6243490.837726hc0.053
67H20H11ax,y,z0.7372550.6111920.790925hc0.053
68H21H11ax,y,z0.6551640.5073690.616027hc0.053
69H22H11ax,y,z0.7312280.6117430.503827hc0.053
70H23H11ax,y,z0.5569380.624290.548772hc0.053
71H24H11ax,y,z0.6307560.7410440.439265hc0.053
72H25H11ax,y,z0.6600890.8007790.554228hc0.053
73H26H11ax,y,z0.4675950.7519190.488001ho0.41
74H27H11ax,y,z0.8308710.8148730.593741hc0.053
75H28H11ax,y,z0.7075470.7970350.56201hc0.053
76H29H11ax,y,z0.7997530.7514670.482203hc0.053
77H30H11ax,y,z0.8531860.5530030.673254ho0.41
78H31H11ax,y,z0.6434770.4423830.782833ho0.41
79H32H11ax,y,z0.4052280.6509710.550787hc0.053
80H33H11ax,y,z0.5921590.6512490.505842hc0.053
81H34H11ax,y,z0.5203670.5489470.324445hc0.053
82H35H11ax,y,z0.5895160.6617780.218959hc0.053
83H36H11ax,y,z0.4141620.6617580.261491hc0.053
84H37H11ax,y,z0.4800810.7866920.159295hc0.053
85H38H11ax,y,z0.5033580.8439180.277684hc0.053
86H39H11ax,y,z0.3159140.7855570.20573ho0.41
87H40H11ax,y,z0.672150.8672260.320813hc0.053
88H41H11ax,y,z0.5508970.8428750.286086hc0.053
89H42H11ax,y,z0.6473390.8061170.205626hc0.053
90H43H11ax,y,z0.7136910.6047650.387334ho0.41
91H44H11ax,y,z0.5117490.4774280.487579ho0.41
92H45H11ax,y,z0.276950.4927770.316273ho0.41
93H46H11ax,y,z0.3127650.2652030.389334ho0.41
94H47H11ax,y,z0.3949140.1327740.598385ho0.41
95H48H11ax,y,z0.2131150.1757330.797958ho0.41
Table A2. PAC.
Table A2. PAC.
Atom #NameElementAtomic numberWycoff
Position
Wycoff
Equation
XYZFF Atom
Type
Charge
1C1C61ax,y,z0.5131630.7226670.454071c2oe0.054
2C2C61ax,y,z0.4789420.6694980.605049c1oe0.107
3C3C61ax,y,z0.3731770.7106240.663953c43o0.107
4C4C61ax,y,z0.2854330.6869120.550835c43o0.107
5C5C61ax,y,z0.2830750.5772450.523724c43o0.107
6C6C61ax,y,z0.388190.5478620.463682coh0.267
7O1O81ax,y,z0.4670660.566360.577042oc−0.32
8O2O81ax,y,z0.3922120.4455720.43524oc−0.32
9C7C61ax,y,z0.5022710.4223120.406015c1oe0.107
10C8C61ax,y,z0.5684490.4215390.558158c1oe0.107
11O3O81ax,y,z0.5338790.3407120.666164oc−0.32
12C9C61ax,y,z0.5214450.2420760.587262coh0.267
13C10C61ax,y,z0.4550820.2508010.441974c43o0.107
14C11C61ax,y,z0.5052780.3226280.332261c43o0.107
15O4O81ax,y,z0.6137520.2923020.295536oh−0.57
16O5O81ax,y,z0.4466870.1522220.369569oh−0.57
17O6O81ax,y,z0.6255780.2025170.54618oh−0.57
18C12C61ax,y,z0.5663820.5237310.651178c2oe0.054
19O7O81ax,y,z0.5820280.6136230.546866oc−0.32
20O8O81ax,y,z0.261660.5244570.670148oh−0.57
21O9O81ax,y,z0.1836880.7201950.613857oh−0.57
22O10O81ax,y,z0.3803450.8185160.687913oh−0.57
23O11O81ax,y,z0.6166910.6820990.380761oc−0.32
24H1H11ax,y,z0.5233510.7999820.478606hc0.053
25H2H11ax,y,z0.4514080.7148940.370873hc0.053
26H3H11ax,y,z0.5355980.6786150.693189hc0.053
27H4H11ax,y,z0.3553060.6761980.772583hc0.053
28H5H11ax,y,z0.3000470.7239870.443468hc0.053
29H6H11ax,y,z0.2237890.5593670.440251hc0.053
30H7H11ax,y,z0.4055840.5879280.359924hc0.053
31H8H11ax,y,z0.5343720.4760540.327749hc0.053
32H9H11ax,y,z0.6485170.406960.526661hc0.053
33H10H11ax,y,z0.4835570.1917380.665519hc0.053
34H11H11ax,y,z0.3780910.2769750.472049hc0.053
35H12H11ax,y,z0.4603980.3248030.227417hc0.053
36H13H11ax,y,z0.6578290.2914580.395134ho0.41
37H14H11ax,y,z0.5022160.145790.283557ho0.41
38H15H11ax,y,z0.6806250.2578740.554148ho0.41
39H16H11ax,y,z0.6297920.5224850.732915hc0.053
40H17H11ax,y,z0.4939540.5299050.714596hc0.053
41H19H11ax,y,z0.3002360.5595030.759677ho0.41
42H20H11ax,y,z0.1544760.6665920.687862ho0.41
43H21H11ax,y,z0.3720350.854210.58293ho0.41
44C13C61ax,y,z0.6387850.6992530.631155c2oe0.054
45C14C61ax,y,z0.7217050.7463250.527925c_10.003
46O12O81ax,y,z0.6936740.7891240.393837o-0
47O13O81ax,y,z0.8330750.7454940.575186o−0.003
48C15C61ax,y,z0.6834340.6181880.484962c2oe0.054
49C16C61ax,y,z0.7671560.5407450.453012c_10.003
50O14O81ax,y,z0.77010.4947220.315753o-0
51O15O81ax,y,z0.8455240.5161380.572953o−0.003
52H22H11ax,y,z0.7440330.663190.435863hc0.053
53H23H11ax,y,z0.6363730.5609310.432774hc0.053
54H24H11ax,y,z0.6753850.6715060.733834hc0.053
55H25H11ax,y,z0.583240.7566030.661779hc0.053
ii-
He-Pycnometry Calculations
N m = N a ρ a V P
where Nm and Na are the number of excess and adsorbed molecules of helium, respectively. VP is the pore volume, and ρa is the density of helium. Under the assumption of zero excess of molecules at such a degree of confinement, the above equation can be used to estimate the pore volume. Then, porosity can be calculated when VP is divided by the bulk volume. A summary of the calculations is given below:
Table A3. Summary of the calculations.
Table A3. Summary of the calculations.
Pressure
(bar)
Density
(g/mL)
Molecular Volume (Å3/molecule) Starch
(molecule/box)
PAC
(molecule/box)
VP starch
(A3)
VP PAC
(A3)
φ Starchφ PAC
0.11.62 × 10−5411000.04.87 × 1043.49 × 10−4200.2143.40.0290.032
0.23.23 × 10−5206000.01.00 × 10−36.91 × 10−4206.0142.30.0300.032
0.34.85 × 10−5137000.01.58 × 10−31.09 × 10−3216.9149.60.0320.034
0.46.46 × 10−5103000.02.11 × 10−31.44 × 10−3216.9148.40.0320.033
0.58.08 × 10−582300.02.54 × 10−31.78 × 10−3209.0146.50.0310.033
0.69.69 × 10−568600.03.02 × 10−32.17 × 10−3207.2148.90.0300.033
0.71.13 × 10−458800.03.64 × 10−32.50 × 10−3214.0147.00.0310.033
0.81.29 × 10−451400.04.09 × 10−32.74 × 10−3210.2140.80.0310.032
0.91.45 × 10−445700.04.52 × 10−33.21 × 10−3206.6146.70.0300.033
11.61 × 10−441200.05.02 × 10−33.53 × 10−3206.8145.40.0300.033

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Figure 1. The particle size distribution of the barite sample (D50 = 30 microns).
Figure 1. The particle size distribution of the barite sample (D50 = 30 microns).
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Figure 2. Experimental apparatus for the static sag test: (a) vertical and (b) inclined (45°) [24].
Figure 2. Experimental apparatus for the static sag test: (a) vertical and (b) inclined (45°) [24].
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Figure 3. Effect of temperature on sag for base fluid under vertical and inclined conditions.
Figure 3. Effect of temperature on sag for base fluid under vertical and inclined conditions.
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Figure 4. Effect of the urea-additive on sag under vertical conditions (250 °F).
Figure 4. Effect of the urea-additive on sag under vertical conditions (250 °F).
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Figure 5. Effect of the urea-additive on sag under inclined conditions, 45° (250 °F).
Figure 5. Effect of the urea-additive on sag under inclined conditions, 45° (250 °F).
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Figure 6. Effect of the urea-additive on the drilling fluid rheology (80 °F).
Figure 6. Effect of the urea-additive on the drilling fluid rheology (80 °F).
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Figure 7. Effect of the urea-additive on the rheological properties of the drilling fluid (80 °F).
Figure 7. Effect of the urea-additive on the rheological properties of the drilling fluid (80 °F).
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Figure 8. Effect of the urea-additive on the yield point–plastic viscosity ratio (80 °F).
Figure 8. Effect of the urea-additive on the yield point–plastic viscosity ratio (80 °F).
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Figure 9. Effect of the urea-additive on the drilling fluid rheology (250 °F).
Figure 9. Effect of the urea-additive on the drilling fluid rheology (250 °F).
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Figure 10. Effect of the urea-additive on the rheological properties of the drilling fluid (250 °F).
Figure 10. Effect of the urea-additive on the rheological properties of the drilling fluid (250 °F).
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Figure 11. Effect of the urea-additive on the filtration performance (250 °F).
Figure 11. Effect of the urea-additive on the filtration performance (250 °F).
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Figure 12. The formed filter cake: (a) base fluid, (b) 0.5 vol.%, and (c) 1.0 vol.%.
Figure 12. The formed filter cake: (a) base fluid, (b) 0.5 vol.%, and (c) 1.0 vol.%.
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Figure 13. Starch (left) and Polyanionic Cellulose (PAC) (right) recreated for molecular simulation.
Figure 13. Starch (left) and Polyanionic Cellulose (PAC) (right) recreated for molecular simulation.
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Figure 14. Two thin layers of (a) starch and (b) PAC formed at 250 °F and 3000 psi.
Figure 14. Two thin layers of (a) starch and (b) PAC formed at 250 °F and 3000 psi.
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Table 1. Summary of the methods used to prevent barite sag.
Table 1. Summary of the methods used to prevent barite sag.
StudyMethodDrilling Fluid SystemFindings
Temple et al., 2004Adding polyalkyl methacrylateOil-basedThe optimum concentration to prevent barite sag was 0.5–3 lb/bbl.
Davis et al., 2017Adding polyethylene glycol (PEG)Oil-basedA concentration of 0.5 lb/bbl was enough to eliminate barite sag.
Basfar et al., 2018 Adding a copolymer Oil-basedA concentration of 1 lbm/bbl of copolymer was enough to prevent barite sag up to 350°F.
Elkatatny, 2019
Boyou et al., 2019Adding nano-silica Water-basedThe cuttings’ transport efficiency was significantly improved in different inclination angles.
Alabdullatif et al., 2015Adding a combination of Mn3O4 and barite as a weighting materialWater-basedMn3O4 effectively enhanced the fluid stability and minimized barite sag.
Mohamed et al., 2017Using micronized bariteWater-basedMicronized barite improved the stability, but it did not eliminate barite sag.
Basfar et al., 2019 Using a barite-ilmenite combined weighting materialWater-basedA proportion of 50 wt.% ilmenite (of the total weighting material) was adequate to prevent barite sag.
Mohamed et al., 2019Oil-basedA proportion of 40 wt.% ilmenite (of the total weighting material) was adequate to prevent barite sag.
Table 2. The elemental composition of the barite sample measured by the X-ray fluorescence (XRF) technique.
Table 2. The elemental composition of the barite sample measured by the X-ray fluorescence (XRF) technique.
Elementwt.%
Si1.9916
S12.6341
K0.6331
Ca0.1109
Fe1.3338
Ni0.0157
Cu0.0354
Sr0.5518
Mo0.017
Ba82.6171
Ta0.023
Pb0.0366
Table 3. The properties and main components of the anti-sagging additive.
Table 3. The properties and main components of the anti-sagging additive.
ParameterDescription
Main components
  • [Pentanoic acid, 5-(dimethylamino)-2-methyl-5-oxo-, methyl ester] 58–59%
  • [Lithium chloride] 1–2%
Density1.11 g/cc
Dynamic viscosity770 mPa.s
Water solubilityCompletely miscible
Flash point> 212 °F
Table 4. Drilling fluid formulation (lab scale).
Table 4. Drilling fluid formulation (lab scale).
ComponentAmount, gMixing Time, minFunction
Water245-Base
Defoamer (D-Air 4000L™)0.081Anti-foam agent
Soda ash0.51Maintains calcium concentration
Xanthan gum polymer1.520Viscosity control
Bentonite410Viscosity control
Potassium hydroxide0.51pH adjustment
Starch610Fluid loss control
PAC-R110Fluid loss control
Potassium chloride2010Clay stabilization
Calcium carbonate510Bridging agent
Barite35010Weighting material
Table 5. Filtration experiment parameters.
Table 5. Filtration experiment parameters.
ParameterDescription
Fluid volume350 cm3
Pressure300 psi
Temperature250 °F
Experiment duration30 min
Ceramic filter disc50-micron
Table 6. Summary of filtration experiments.
Table 6. Summary of filtration experiments.
ParameterBase Fluid0.5 vol.%1.0 vol.%
Filtrate volume, cm39.61110.7
Filter cake weight, g29.134.9429.77
Filter cake thickness, mm3.64.23.6

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Mohamed, A.; Al-Afnan, S.; Elkatatny, S.; Hussein, I. Prevention of Barite Sag in Water-Based Drilling Fluids by A Urea-Based Additive for Drilling Deep Formations. Sustainability 2020, 12, 2719. https://doi.org/10.3390/su12072719

AMA Style

Mohamed A, Al-Afnan S, Elkatatny S, Hussein I. Prevention of Barite Sag in Water-Based Drilling Fluids by A Urea-Based Additive for Drilling Deep Formations. Sustainability. 2020; 12(7):2719. https://doi.org/10.3390/su12072719

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Mohamed, Abdelmjeed, Saad Al-Afnan, Salaheldin Elkatatny, and Ibnelwaleed Hussein. 2020. "Prevention of Barite Sag in Water-Based Drilling Fluids by A Urea-Based Additive for Drilling Deep Formations" Sustainability 12, no. 7: 2719. https://doi.org/10.3390/su12072719

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