Development and Evaluation from Laboratory to Field Trial of a Dual-Purpose Fracturing Nanofluid: Inhibition of Associated Formation Damage and Increasing Heavy Crude Oil Mobility
Abstract
:1. Introduction
2. Materials and Methods
2.1. Materials and Chemicals
2.2. Methods
2.2.1. Nanoparticle Surface Modification
2.2.2. Nanoparticle Characterization
2.2.3. Preparation of the Fracturing Fluids
2.2.4. Rheological Experiments
- The first kind of test related to low-pressure conditions was performed using a Kinexus Pro+ rotational rheometer (Malvern Instruments, Worcestershire, UK) with a Peltier plate for temperature control. At first, the viscosity changes in the HO induced by the presence of the nanoparticles were evaluated. In this case, a low (100 mg/L) and a high (1000 mg/L) concentration of these were mixed with the crude oil by stirring at 500 rpm for 30 min until homogenization [7]. The measures were made using a plate-plate geometry at a gap of 300 μm at 25 °C in a shear rate range of 1 to 100 s−1.
- Other tests at low pressure were carried out to determine if nanomaterials tend to aggregate in the presence of ZPM, as the proppant does. For this purpose, the LG was tested in the presence and absence of ZPM with or without the different nanoparticles at a concentration of 1000 mg/L. This set of rheological measurements was made with the geometry of the solid cylinders at 25 °C at a shear rate between 1 and 100 s−1. As mentioned above, the FF viscosity is one of the main properties of this kind of fluid due to its importance in placing the proppant in the open fracture according to the plan [27,33]. Hence, rheological measures were made to the original FF and samples of this when adding 100 and 1000 mg/L of the different nanoparticles. The solid cylinders geometry was used at the same temperature and fixed shear rates of 25, 50, 75 and 100 s−1. The purpose of this test is to emulate at low pressures and temperatures the first effort of the API RP39 test [34], the standard for evaluating the rheological properties of the fracturing fluids.
- Precisely, this is the third type of test, and a high pressure—high temperature Chandler 5550 viscometer (Chandler Engineering, Broken Arrow, USA) was used at the expected reservoir and fracking conditions 77 °C and 5500 psi. This procedure allows following the viscosity of the evaluated fracturing fluids when arming and through their rupture process under the action of shear rates of 25, 50, 75 and 100 s−1.
2.2.5. Wettability Alteration
2.2.6. Equilibrium Adsorption Isotherms of Polymer over the Rock Surface
2.2.7. Core-Flooding Tests
2.2.8. Field Trial in a Colombian Oilfield
2.3. Modelling
2.3.1. Rheological Model
2.3.2. SLE Model
3. Results
3.1. Nanoparticles Characterization and Selection of the Best according to Their Capacity of Enhancing HO Mobility
3.1.1. Nanoparticles Characterization
3.1.2. Crude Oil Viscosity Reduction
3.1.3. Nanoparticle Wettability Alteration
3.2. Static Tests of Adding Nanoparticles to a Commercial FF
3.2.1. Linear Gel
3.2.2. FF and Interactions Polymer-Nanoparticles
3.2.3. Optimized Fracturing Nanofluid
3.3. Dynamic Tests Made to Original FF and Optimized NanoFF
3.3.1. Proppant Media Tests
3.3.2. Formation Core Tests
3.4. Field Application in the Castilla Oil Field
4. Conclusions
Author Contributions
Funding
Institutional Review Board Statement
Informed Consent Statement
Data Availability Statement
Acknowledgments
Conflicts of Interest
References
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Sample | Core | Carbolite Porous Media |
---|---|---|
Length (cm) | 6.8 ± 0.1 | 7.2 ± 0.1 |
Diameter (cm) | 3.7 ± 0.1 | 3.8 ± 0.1 |
Porosity (%) | 21.8 ± 0.2 | 26.4 ± 0.2 |
Effective permeability to water (mD) | 14.5 ± 0.2 | 477 ± 3 |
Effective permeability to oil (mD) | 1372 ± 4 | 13,995 ± 9 |
Order | Additive | Dosage % v/v |
---|---|---|
1 | Bactericide | 0.005 |
2 | Clay stabilizer | 0.200 |
3 | Guar gum-based polymer | 0.875 |
4 | Surfactant | 0.200 |
5 | Zeta Potential Modifier | 1.500 |
6 | pH controller | 0.400 |
7 | Delayed breaker | 0.400 |
8 | Peroxide breaker | 0.100 |
9 | Metaborate crosslinker | 480 mg/L |
Nanoparticle | dp-50 ± 0.2 nm | SBET ± 1 m2/g | Total Acidity ± 0.02 mmol/g | Isoelectric Point ± 0.03 (pH) |
---|---|---|---|---|
Si07 | 11.6 | 388 | 2.16 | 2.40 |
Si07A | 12.9 | 216 | 2.85 | 2.05 |
Si07B | 13.4 | 143 | 1.29 | 2.25 |
Si200 | 37.2 | 303 | 1.99 | 2.35 |
Si200A | 39.7 | 182 | 2.91 | 1.95 |
Si200B | 43.1 | 106 | 1.46 | 2.05 |
Al | 95.0 | 103 | 0.61 | 9.70 |
Al-A | 97.2 | 76 | 0.77 | 6.42 |
Al-B | 97.4 | 62 | 0.59 | 7.38 |
Parameter | HO | Si07 100 ppm | Si07 1000 ppm | Si200 100 ppm | Si200 1000 ppm | Al 100 ppm | Al 1000 ppm |
---|---|---|---|---|---|---|---|
µ(∞,γ) (cP) | 21,497.76 | 20,953.69 | 18,617.21 | 21,884.76 | 21,157.80 | 21,701.18 | 21,698.76 |
µ(0,γ) (cP) | 87,857.79 | 85,926.09 | 77,621.58 | 86,881.78 | 86,044.27 | 86,847.72 | 84,335.92 |
αc (s) | 0.0205 | 0.0213 | 0.0202 | 0.0209 | 0.0210 | 0.0209 | 0.0217 |
m | 2.55 | 2.36 | 2.33 | 2.61 | 2.61 | 2.65 | 2.67 |
RSME% | 3.74 | 4.78 | 4.13 | 4.88 | 4.86 | 4.38 | 4.47 |
DVR% (@ 10 s−1) | - | 3.41 | 10.95 | 1.24 | 2.42 | 0.26 | 0.61 |
Parameter | HO | Si07B 1000 ppm | Si07A 1000 ppm | Si200B 1000 ppm | Si200A 1000 ppm | Al-B 1000 ppm | Al-A 1000 ppm |
---|---|---|---|---|---|---|---|
µ(∞,γ) (cP) | 21,497.76 | 20,901.40 | 20,519.24 | 21,843.35 | 21,331.19 | 20,486.17 | 21,557.05 |
µ(0,γ) (cP) | 87,857.79 | 83,590.54 | 82,053.06 | 87,101.90 | 87,267.08 | 85,215.54 | 87,697.57 |
αc (s) | 0.0205 | 0.0206 | 0.0207 | 0.0205 | 0.0211 | 0.0207 | 0.0208 |
m | 2.55 | 2.56 | 2.60 | 2.63 | 2.61 | 2.62 | 2.57 |
RSME% | 3.74 | 3.63 | 4.08 | 4.46 | 4.92 | 4.37 | 4.01 |
DVR% (@ 10 s−1) | - | 3.69 | 6.50 | 0.89 | 1.27 | 0.81 | 2.76 |
Shear Rate (s−1) | µ FF (cP) | µ FF + Si07 (cP) | DVR% | µ FF + Si200 (cP) | DVR% | µ FF + Al (cP) | DVR% |
---|---|---|---|---|---|---|---|
25 | 1850 ± 2 | 2406 ± 3 | 30.1 | 3453 ± 3 | 86.6 | 2376 ± 3 | 28.4 |
50 | 1332 ± 2 | 1327 ± 2 | 0.4 | 1611 ± 3 | 20.9 | 1521 ± 2 | 14.2 |
75 | 998 ± 1 | 1 078 ± 2 | 8.0 | 1184 ± 2 | 18.6 | 1260 ± 2 | 26.3 |
100 | 915 ± 1 | 913 ± 1 | −0.2 | 954 ± 1 | 4.2 | 955 ± 1 | 4.4 |
H (mg/m2) | K (g/g) | q (mg/g) | RSME% |
---|---|---|---|
0.037 | 0.072 | 5.75 | 3.99 |
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Giraldo, M.A.; Zabala, R.D.; Bahamón, J.I.; Ulloa, J.M.; Usurriaga, J.M.; Cárdenas, J.C.; Mazo, C.; Guzmán, J.D.; Lopera, S.H.; Franco, C.A.; et al. Development and Evaluation from Laboratory to Field Trial of a Dual-Purpose Fracturing Nanofluid: Inhibition of Associated Formation Damage and Increasing Heavy Crude Oil Mobility. Nanomaterials 2022, 12, 2195. https://doi.org/10.3390/nano12132195
Giraldo MA, Zabala RD, Bahamón JI, Ulloa JM, Usurriaga JM, Cárdenas JC, Mazo C, Guzmán JD, Lopera SH, Franco CA, et al. Development and Evaluation from Laboratory to Field Trial of a Dual-Purpose Fracturing Nanofluid: Inhibition of Associated Formation Damage and Increasing Heavy Crude Oil Mobility. Nanomaterials. 2022; 12(13):2195. https://doi.org/10.3390/nano12132195
Chicago/Turabian StyleGiraldo, María A., Richard D. Zabala, Jorge I. Bahamón, Juan M. Ulloa, José M. Usurriaga, José C. Cárdenas, Camilo Mazo, Juan D. Guzmán, Sergio H. Lopera, Camilo A. Franco, and et al. 2022. "Development and Evaluation from Laboratory to Field Trial of a Dual-Purpose Fracturing Nanofluid: Inhibition of Associated Formation Damage and Increasing Heavy Crude Oil Mobility" Nanomaterials 12, no. 13: 2195. https://doi.org/10.3390/nano12132195
APA StyleGiraldo, M. A., Zabala, R. D., Bahamón, J. I., Ulloa, J. M., Usurriaga, J. M., Cárdenas, J. C., Mazo, C., Guzmán, J. D., Lopera, S. H., Franco, C. A., & Cortés, F. B. (2022). Development and Evaluation from Laboratory to Field Trial of a Dual-Purpose Fracturing Nanofluid: Inhibition of Associated Formation Damage and Increasing Heavy Crude Oil Mobility. Nanomaterials, 12(13), 2195. https://doi.org/10.3390/nano12132195