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Emulsification flooding can effectively enhance crude oil recovery to solve the problem of petroleum shortage. In this work, a modified Janus Nano Calcium carbonate (JNC-12) with a particle size of 30-150 nm was synthesized, and an in situ emulsification nanofluid (ISEN) was prepared with JNC-12 and alkyl polyglycoside (APG). Scanning electron microscope (SEM) showed that the dispersion of JNC-12 in air or APG solution was better than Nano Calcium carbonate (Nano CaCO3). The emulsification properties, interfacial tension, and expansion modulus of ISEN were studied, and the result showed that with the increase in salinity, the emulsification rate decreased, the water yield rate increased, the interfacial tension first decreased and then increased, and the expansion modulus first increased and then decreased. With the increase in temperature, the emulsification rate, emulsion viscosity, and interfacial tension decreased. With the increased oil-water volume, the water yield rate and the emulsion viscosity increased. With increase in the concentration of JNC-12, the water yield rate, the emulsion viscosity, and the interfacial tension decreased but the expansion modulus increased. The emulsion generated by emulsifying ISEN with crude oil was an O/W emulsion, the crude oil viscosity was 4-10 times that of emulsion, and the average particle size of emulsion was 1.107 µm. The addition of ISEN caused the decrease in interfacial tension of oil-water to 0.01-0.1 mN/m. The wettability alteration experiment found that ISEN could change the lipophilic rock to hydrophilic rock. Finally, the core displacement experiments showed that compared with the first water flooding, the oil recovery of the second water flooding after ISEN flooding enhanced by 17.6%. This research has important guiding significance for in situ emulsified nanofluid flooding to enhance oil recovery.
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Nowadays, high-phase-inversion in situ emulsification technology has shown great potential in enhancing oil recovery from high-water-cut thin-oil reservoirs. However, emulsification characteristics, interfacial properties, and the mechanism of high phase inversion have not been systematically described. In this study, an emulsification experiment was conducted to investigate the effects of shear time, shear rate, and temperature on the phase inversion of thin oil. Furthermore, the influence of resin and wax on the dispersion of asphaltene was studied through microscopic morphology analysis. Interfacial tension measurement and interfacial viscoelasticity analysis were carried out to determine the interaction characteristics of asphaltene, resin, and wax at the interface. The results showed that, at 50 °C, the phase-inversion point of thin oil reached as high as 75%, and even at 60 °C, it remained at 70%. The shear time and shear rate did not affect the phase-inversion point of thin oil, while an increase in temperature led to a decrease in the phase-inversion point. Moreover, compared to the 20% phase-inversion point of base oil, the phase-inversion point increased with different proportions of asphaltene, resin, and wax. Particularly, at the ratio of asphaltene/resin/wax = 1:5:9, the phase-inversion point reached as high as 80%, indicating the optimal state. In this proportion, asphaltene aggregates exhibited the smallest and most uniform size, best dispersion, lower interfacial tension, and higher interfacial modulus. These findings provide reference and guidance for further enhancing oil recovery in medium-to-high-water-cut thin-oil reservoirs.
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In this study, a piperazinyl-based emulsifier (EA/AMPA) was synthesized to prepare water-in-oil (W/O) high internal phase emulsions (HIPEs). Using kerosene as the oil phase, stable HIPEs with internal phase fractions of up to 98% were prepared. This enabled the EA/AMPA to have a high efficiency, as the HIPEs with a 90% internal phase fraction could be easily prepared with 0.1% of EA/AMPA. In addition, the formation of HIPEs was not affected by the addition of Na+. Because of the fact that EA/AMPA has a hydrophilic head with two tertiary amines, EA/AMPA could be easily recovered from the oil phase by adjusting the pH to acidic values. Moreover, the unique structure promoted the formation of stable HIPEs, even with crude oil used as the oil phase. The results indicate that EA/AMPA has the potential to significantly contribute to the preparation of W/O HIPEs and that the design of the hydrophilic head with two tertiary amines can provide a reference for the fabrication of new W/O emulsifiers.
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The structure of amphiphilic spherical brushes, consisting of the nano-SiO2 core, the hyperbranched polyamidoamine subshell, and a grafted layer of long hydrophobically modified polyacrylamide (HMPAM) chains, in aqueous solution was analyzed and described in the framework of the original mean-field approach. The scaling estimations of the hydrodynamic radius of such polymer brushes as a function of the number of grafted macromolecules allow concluding that the HMPAM shells are in a globular state and that the region of the stretched chains adjacent to the grafting surface is a minor part of the grafted macromolecules and does not have a significant impact on the self-assembly of the HMPAM shell caused by the complex hydrophobic-hydrophilic composition of their monomer units. In mean-field theory, the amphiphilic nature of HMPAM was taken into account by attaching the hydrophobic side group H to some fraction of monomer units of the hydrophilic P backbone. The strong attraction of H groups causes the aggregation of macromolecules, whereas the affinity of hydrophilic P groups to solvent forces the aggregates to increase their surface. Due to such effective surface activity, in poor solvent, the grafted amphiphilic macromolecules could form a spherical compacted structure around the nanoparticle or self-assemble into a "hedgehog" structure with several "spines" having hydrophobic core and hydrophilic shell. State diagrams, obtained theoretically, reveal that the "hedgehog" structure is preferable for a wide range of energetic parameters.
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The surface hydrophobicity of solid particles plays a critical role in the nucleation of gas hydrate formation, and it was found that the hydrophobic surface will promote this nucleation process, but the underlying mechanism is still unveiled. Herein, we proposed for the first time our new theory that the formation of methane nanoscale gas bubbles on the hydrophobic surface provides the nuclei sites for further formation of methane hydrate. First, we studied the effect of hydrophobicity of particles on the nucleation of hydrate. It was found that the hydrophobic graphite and silica particles would promote the nucleation of hydrate, but the hydrophilic silica particles did not promote the methane hydrate nucleation. Then, we designed the atomic force microscopy experiment to explain this mechanism from a nanometer scale. The results showed that the methane nanobubbles were formed on the hydrophobic highly ordered pyrolytic graphite surface, but they were hard to form on the hydrophilic mica surface. These results indicated that the methane nanobubbles on the hydrophobic surface could provide the gas hydrate nucleation sites and may induce a rapid nucleation of methane hydrate.
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To solve the potential risk of present oilfield chemistries to subterranean environment, our group contributes to the development of "green" petroleum production processes. This proof-of-concept research studied the well-defined nanocellulose-based nanofluids, i.e., original (NC), AMPS grafted (NC-KY), and AMPS and hydrophobic chains grafted (NC-KYSS), in stabilizing foam lamella for potential use in enhanced oil recovery (EOR). The data showed that the collaboration of the surface-functional nanocellulose considerately improved the foam stability particularly in the presence of hydrocarbons due to the thickened foam film coupled with the molecular interactions at interior lamella. Since the grafted AMPS and alkyl chains, NC-KYSS noticeably enhanced foam quality compared against NC and NC-KY. With the increase in gas pressure, the lamella stabilizing effect of NC-KYSS became increasingly significant. The coflowing behaviors of foam with oleic phase in porous media were examined in a five-spot visualization micromodel (15 cm × 15 cm × 1 cm) and identified using a digital analysis method. The defoaming/destabilizing effect of hydrocarbons was fairly notable in porous media, causing the foam to finger through the formed "oil bank". However, a tough displacement front was constructed when the surfactant synergized with NC-KYSS due to the stabilized foam lamella and 12% of incremental oil recovery was produced.
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A molecularly dispersed nano-material called POSS-NH2-AA was synthesized to construct a hybrid hydrogel with a rapid self-healing ability (stress 8 kPa) and excellent mechanical performance (a strain of 4683% and a stress of 37.8 kPa). The hydrogel also exhibits good cohesiveness to materials, such as plastics, glass and iron. The backbone of the POSS makes the hydrogel much stronger than the hydrogel without POSS, which accounts for the improvement in its properties. This process is facile and useful to construct mechanically strong and self-healable materials.
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Fracturing flowback fluid (FFF) including various kinds of organic pollutants that do harms to people and new treatments are urgently needed. Advanced oxidation processes (AOPs) are suitable methods in consideration with molecular weight, removal cost and efficiency. Here, we summarize the recent studies about AOP treatments towards organic pollutants and discuss the application prospects in treatment of FFF. Immobilization and loading methods of catalysts, evaluation method of degradation of FFF, and continuous treatment process flow are discussed in this review. In conclusion, further studies are urgently needed in aspects of catalyst loading methods, macromolecule organic evaluation methods, industrial process, and pathways of macromolecule organics' decomposition.
Assuntos
Poluentes Químicos da Água , Humanos , Oxirredução , CatáliseRESUMO
Carbon dioxide (CO2) flooding is a promising method for developing low-permeability heterogeneous glutenite reservoirs (LPHGRs) featured with low natural energy. Herein, the focus of this work was to study the microscopic oil displacement mechanism of CO2 in LPHGRs. First, the micropore structure and mineral composition of LPHGRs were analyzed, and the effect of CO2 on low-permeability reservoirs was then studied. Also, the mechanism of CO2 displacement in low-permeability reservoirs on a pore scale was analyzed using nuclear magnetic resonance technology in different dimensions. The experimental results showed that the mineral composition of the rock mainly included quartz, feldspar, and clay minerals. The core pores were poorly developed and highly heterogeneous. The clay and other mineral particles produced by the dissolution reaction of rocks and minerals migrated and deposited with formation fluid to damage the reservoir. On the contrary, it also improved the pore structure, increased pore space, and increased reservoir permeability. The miscible interaction between CO2 and crude oil formed a stable displacement front, which enabled crude oil to be well displaced from the macropores and medium pores. However, this interaction generated negligible effects on the small pores. The experimental results provided important indicators for CO2 development in LPHGRs.
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A tight conglomerate reservoir is a kind of unconventional reservoir with strong heterogeneity, and CO2 injection is an economical and environmentally friendly method to enhance tight oil recovery. Supercritical CO2 is a very promising fluid medium for unconventional reservoir development due to its gas-liquid dual properties. In this study, the production effects of supercritical CO2 and non-supercritical CO2 in tight conglomerate reservoirs were quantitatively analyzed by huff and puff simulation experiments conducted under reservoir conditions (formation pressure 37 MPa, temperature 89 °C). Also, the influencing factors of CO2 huff and puff production, including injection volume, soaking time, and throughput cycles, were investigated. The results showed that supercritical CO2 improves the recovery by 4.02% compared with non-supercritical CO2. It could be seen that supercritical CO2 plays a positive role in improving tight conglomerate reservoirs. The optimal injection volume, soaking time, and throughput cycles were determined to be 0.50 PV, 2 h, and 3 cycles, respectively. This paper provides an important basis for the study of supercritical CO2 production in tight conglomerate reservoirs.
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On account of the intralayer and interlayer heterogeneity, high temperature (110 °C), and high salinity (224,919 mg/L) of Tahe channel sand reservoir, single profile control or chemical flooding cannot greatly enhanced oil recovery. The goal of the current research was to optimize a polymer gel formula that was suitable for high-temperature and high-salinity reservoirs, screen an appropriate chemical flooding method, and determine the efficiency of the combination of profile control and chemical flooding. Experimental results indicated that the formed polymer gel could maintain relatively high strength after aging for 30 days. Moreover, the combination of profile control and surfactant flooding could result in an enhanced oil recovery of 17.9%, and the combination of profile control and foam flooding could result in an enhanced oil recovery of 23.0%, which was ascribed to the improvement of sweeping efficiency and displacement efficiency. All the results indicated that the formed polymer gel and the combination of profile control and chemical flooding have great application potential in Tahe high-temperature and high-salinity channel sand reservoir.
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This proof-of-concept study demonstrates a facile and scalable 'dry water' method for producing micrometer-sized microgel particles by use of 'water-in-air' droplets as micro-reactors. Solid microgel particles could be easily produced by this method with no further purification. The microgel particles comprise of porous hydrophobic shells and hydrophilic cores and could absorb both oil and water. The swelling of the particles could be triggered by a surfactant under a wide range of conditions.