Recent Advances of Graphene-Derived Nanocomposites in Water-Based Drilling Fluids
Abstract
:1. Introduction
2. Role of Significant Nanocomposites in Drilling Fluids
2.1. Effect of Silica Nanocomposites
2.2. Effect of Copper Oxide Nanocomposites
2.3. Role of Titanium Dioxide Nanocomposites
2.4. Effect of Grass and Other Additives to Improve Rheological Properties
2.5. Applications of Various Nanocomposites in Drilling Fluids
3. Variation of Rheological Properties by Nanocomposites
3.1. Gel Strength
3.2. Filtrate Loss
3.3. Shear Rate
4. Graphene Impacts in Drilling Operations
4.1. Graphene-Derived Nanocomposites in WBDF
4.1.1. Graphene-Polymer Nanocomposites
4.1.2. Graphene-Activated Carbon Nanocomposites
4.1.3. Graphene-Metal Nanocomposites
4.1.4. Graphene-Metal Oxide Nanocomposites
4.1.5. Graphene-Fiber Nanocomposites
Graphene-Derived Nanocomposites | Synthesis Routes | Conditions & Outcomes | References |
---|---|---|---|
Graphene-polypropylene (PP) nanocomposite | Melt mixing | Enhanced PV versus SR, 20~5000 s−1 for nanocomposites at 200 °C. The PV of PP was observed 289 Pa s at 300 s−1 SR, which increased up to 513 Pa s due to the stronger interaction of the PP matrix with GO nanocomposite. | [107] |
Graphene-acrylonitrile butadiene styrene resin (ABC) nanocomposite | Facile coagulation method | An increase of PV and mechanical modulus was observed due to the graphene nanocomposite. | [108] |
Graphene-polyester nanocomposite | Partial pyrolysis | An enriched RP was observed due to the nanocomposite as compared to graphite. | [109] |
Graphene-polyurethane nanocomposite | Solution mixing method | 0.5–3 wt.% qualitative expansion was presented in the frequency of RP. | [110] |
Graphene-low density polyethylene nanocomposite | Melt extrusion and film casting | Established PV, ST, viscoelasticity at 140 ℃. | [111] |
GO-Fe2O3/Al2O3 nanocomposite | Vertical bed method | Nanocomposite reduced the FL from 20 mLto 15 mL and MCT from 0.3 mm to 0.1 mm of WBDF with 0.02%. | [112] |
GO-ZrO nanocomposite | Microwave synthesis | Enriched HPHT applications using a high-temperature range of 330 °F. | [113] |
rGO-SnO2 nanocomposite | Ultrasonic synthesis | Improved RPs were reported with the effect of vol% of rGO–SnO2 nanocomposite (three different ratios: 1:7, 1:8, 1:10) in base fluid for PV, ST, ranging from 0 to 10,000 s−1 at 25 °C. | [114] |
GO-ZnO nanocomposite | Chemical synthesis | A desirable increase of PV (5–28%), YP (25–42%), GS (25–33%), and a considerably reduced FL were examined. | [66] |
rGO-thermally polypyrrole nanocomposite | In situ polymerization | RP of rGO-thermally polypyrrole nanocomposite was determined using a cone-plate method with ratios (100:1, 100:3, and 100:5%) and temperature (25–180 °C), and represented an increase of ST and PV due to the addition of thermally reduced GO sheets into polypyrrole. | [115] |
GO-polyacrylamide (PAM) nanocomposite | Chemical synthesis (polymerization) | Nanocomposite influenced FL at LPLT and HPHT which was reduced up to 38.96% and 34.36, respectively. A noteworthy decrease in FL, MCT treated with 1.5 wt.% nanocomposite. | [116] |
GO-hydrolyzed polyacrylamide nanocomposite | Chemical synthesis | Addition of GO increased PV, the effect was notable at elevated temperatures. Addition of 0.1 wt.% of GO enhanced PV by 47% and 36%, respectively, at 85 °C and 25 °C. GO increased the thermal stability due to the electrostatic hydrogen bonding among nanocomposite functional groups. After ageing for 30 days at 80 °C, PV of the composite’s solution decreased very slightly, while a 59% reduction was observed for pure polymer solution. | [117] |
GO nanocomposite | Chemical synthesis | Reduced FL was observed using low concentration of GO nanocomposite. | [118] |
Applications of Other Graphenaceous Materials in WBDF | |||
GO/polyanionic cellulose polymers | Hummers method | FL of 6.1 mL over 30 min, MCT ~20µm/FL of 7.2 mL, MCT ~280 µm, high-temperature stability with better-quality RP. | [16] |
GO | Hummers method | Concentration of GO increased from 0.2 wt.% to 0.6 wt.%, PV of GO aqueous dispersion noticeably increased, whereas there was no obvious change of YP and GS. | [119] |
GNP | Hydrothermal technique | Amended RP was presented at HPHT due to the low friction between nanoplates. | [28] |
Graphene/MgO/TiO2 | Hydrothermal technique | An increase of GS (92%) and PV (253%) by adding MgO (2%) and graphene (75%) was observed. | [120] |
Graphite–Al2O3 | - | Upgraded drilling mud properties were revealed; thermal conductivity (10%) and zeta potential (13%) in the presence of 0.8 wt.% of graphite-Al2O3. | [121] |
Graphene | - | Graphene with a concentration of 17.5 mL was reduced polymer usage up to 40% for mud cake formula. Better-quality RP of 13.5lb/gal HPHT was achieved in WBDF without affecting PV and YP. | [122] |
Graphitized nanotubes | Homogenization | Decrease of PV with an increase in temperature from 25–85 °C. Value-added RP with an increase of temperature were presented. | [123] |
Nano-graphite nanoparticles | Water-in-oil (w/o) micro emulsions | Decrease in FL and RP were enhanced for WBDF. | [124] |
Graphene/CNT | Chemical method | Reduced mud filtrate volume up to 18%. Addition of CNT reduced FL, enhanced shale formation. Addition of graphene was decreased friction coefficient from 38–59%. Better lubricity was produced by CNT as compared to graphene at elevated temperature. | [125] |
Graphene–SiO2 | - | Concentration of nanoparticles (0.75 wt.%) yielded better performance in both LPLT and HPHT filtration tests with a reduction of 20.93% and 27.21%, respectively, as compared to the base fluid. | [126] |
GO-phosphorylated from welding waste | Chemical synthesis | Addition of GO was tested for improved RP such as PV was reduced from 10 to 7 cp, YP was increased from 11–15 lbs/100 ft2, decreased filtrate volume (6 to 3.6 mL) and reduced MCT (1.06 to 0.33 mm), with enhanced lubricity were presented. | [127] |
4.2. Graphene Oxide on Rheological Properties
4.3. Graphene Oxide in WBDF
5. Limitations and Challenges
6. Future Prospects
7. Conclusions
Author Contributions
Funding
Acknowledgments
Conflicts of Interest
References
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Nanocomposites | Experimental Conditions | Rheological Properties | Outcomes | References |
---|---|---|---|---|
Nanosilica polymer composite | LPLT and high temperature up to 446 °F | PV, YP, GS, FL, MCT | Under LPLT conditions, the usage of nanosilica (1.0 wt.%) has greatly enhanced the rheological and filtration properties. Nanocomposites have shown no decomposition under high temperatures at 392, 410, 428, and 446 °F, proving nanocomposites to be suitable under HPHT conditions. | [17] |
ZnO nanocomposite | HPHT at 109 to 370 °F and 150 to 18,500 psi | PV, YP | 2.3 wt.% of ZnO nanocomposite (5 to 50 nm) resulted in upgrading the rheological properties under HPHT conditions. | [27] |
TiO2-polyacrylamide | LPLT | PV, YP, GS, FL | Development in rheological properties and filtration behavior under LPLT condition was observed by using 1–14 g of TiO2-PAM nanocomposite. | [26,48] |
ZnO-polyacrylamide | At 80 and 150 °F | PV, AV, YP, GS, FL | By adding 0.8 g of ZnO-PAM nanocomposite in the drilling fluid, PV and YP increased by 18.8% and 16.7%, respectively. Fluid loss was reduced by 12.7% and 23% under LPLT and HPHT conditions, respectively, when using 1 g of nanocomposite. | [28] |
Sepiolite | LPLT and HPHT at 122 to 356 °F and 500 to 6000 psi | - | The experiment showed that WBDF samples with 1.4 wt.% of sepiolite enriched the rheological properties at 6000 psi and temperatures up to 356 °F conditions. | [49] |
Polyacrylamide-grafted polyethylene glycol nanosilica | High temperature up to 203 °F | PV, YP, GS, FL | Enhancement of rheological and filtration properties was observed with 0.7 wt.% of nanocomposite and the values remained stable under a temperature of 203 °F. | [50] |
Hydrophobic modified polymer-based silica | LPLT | PV, YP, GS, FL | Rheological and filtration properties were improved by adding 2.0 wt.% before and after hot rolling under 250 °F for 16 h. | [51] |
Polyethylene glycol grafted nanosilica | LPLT | PV, AV, YP, GS, FL | Results have showed that PV, YP, and AV values were increased while fluid loss volume was decreased to 15.2% by adding 1 g of nanocomposite in drilling fluid. | [52] |
Amphiphilic polymer/nano-silica | LPLT | PV, AV, YP, GS, FL | PV was enhanced by the addition of 7.1% nanocomposite. Addition of 2 wt.% nanocomposite reduced the fluid loss volume to 6.4 mL. | [53] |
Nanocarboxylmethyl cellulose/polystyrene core-shell nanocomposite | LPLT | PV, AV, YP, GS, FL | PV and AV increased by up surging the concentration of three additives. YP values were the highest for bulk CMC while core-shell nanocomposites recorded the lowest amount of fluid loss volume. | [24] |
CuO/ZnO/synthetic polymer nanocomposite | LPLT and high temperature up to 400 °F | PV, YP, GS, FL, MCT | The drilling fluid exhibited stable rheological and filtration properties at 400 °F. Under LPLT conditions, low fluid loss volume was recorded. while the mud cake formed was thin and impermeable. | [54] |
Lignosulfonate/Acrylamide graft copolymers | 78 °F and 250 °F | PV, YP, GS, FL, MCT | At a temperature of 78 °F and 250 °F, rheological and filtration properties of the drilling fluid were enhanced with the inclusion of nanocomposite (2.4–3.5 g/350 mL water). | [55] |
Hybrid polymer nanocomposite poly(styrene-methylmethacrylate-acrylic acid)/nanoclay | High temperature up to 250 °F | PV, YP, GS, FL | The nanocomposite presented stable rheology at temperatures up to 250 °F, and the combination of nanocomposite in nanoclay-based drilling fluid was reduced by up to 22% fluid loss under LPLT conditions, and a 65% reduction in the polymer-based drilling fluid. | [56] |
Novel synthetic based acrylamide-styrene copolymer | High temperature up to 250 °F | PV, YP, GS, FL, MCT | Rheological and filtration properties proved a progressive fluid loss control. An ideal filtration performance at LPLT and HPHT conditions was achieved with the addition of 3 g of nanocomposite into the drilling fluid. | [57,58] |
Synthesis Routes | Nanofiller Content | Advantages | Limitations |
---|---|---|---|
In situ polymerization | 5–70 wt.% | Fabrication and polymerization occur at the same time to produce an efficient interface between filler and polymer | Suitable for limited types of polymers |
Shear press | 60–70 wt.% | Fine alignment | Restricted to small-scale production |
Vacuum-assisted polymer infiltration | 5–70 wt.% | Competent at producing large and complex composites | Filler fractions and thickness are challenging to control |
Spray winding | 50–80 wt.% | Satisfactory alignment and large-scale production | Comparatively complex apparatus |
Capillary rise infiltration | 40–60 wt.% | User-friendly apparatus | Limited to thermoplastic polymers |
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Ikram, R.; Mohamed Jan, B.; Vejpravova, J.; Choudhary, M.I.; Zaman Chowdhury, Z. Recent Advances of Graphene-Derived Nanocomposites in Water-Based Drilling Fluids. Nanomaterials 2020, 10, 2004. https://doi.org/10.3390/nano10102004
Ikram R, Mohamed Jan B, Vejpravova J, Choudhary MI, Zaman Chowdhury Z. Recent Advances of Graphene-Derived Nanocomposites in Water-Based Drilling Fluids. Nanomaterials. 2020; 10(10):2004. https://doi.org/10.3390/nano10102004
Chicago/Turabian StyleIkram, Rabia, Badrul Mohamed Jan, Jana Vejpravova, M. Iqbal Choudhary, and Zaira Zaman Chowdhury. 2020. "Recent Advances of Graphene-Derived Nanocomposites in Water-Based Drilling Fluids" Nanomaterials 10, no. 10: 2004. https://doi.org/10.3390/nano10102004
APA StyleIkram, R., Mohamed Jan, B., Vejpravova, J., Choudhary, M. I., & Zaman Chowdhury, Z. (2020). Recent Advances of Graphene-Derived Nanocomposites in Water-Based Drilling Fluids. Nanomaterials, 10(10), 2004. https://doi.org/10.3390/nano10102004