Development of Novel Silicon Quantum Dots and Their Potential in Improving the Enhanced Oil Recovery of HPAM.

Hydrolyzed polyacrylamide (HPAM) is commonly used in polymer flooding, however, it is prone to viscosity reduction at high temperatures and high salinities, weakening its ability to improve oil recovery. In this work, sulfonated modified silicon quantum dots (S-SiQDs) were synthesized and then added to HPAM to study the improvement of rheological properties and enhanced oil recovery performance of HPAM at high temperatures and salinities. It is found that the S-SiQDs with a concentration of only 0.1 wt % can significantly increase the viscosity of HPAM from 28.5 to 39.6 mPa·s at 60 °C and 10,000 mg/L NaCl. Meanwhile, the HPAM/S-SiQDs hybrid solution always possessed higher viscosity and viscoelastic moduli than HPAM, attributed to the hydrogen bonding between HPAM and S-SiQDs. Notably, HPAM/S-SiQDs still maintained elastic behavior at harsh conditions, indicating that they formed a strong network structure. Through oil displacement experiments, it was found that the oil recovery of HPAM/S-SiQDs was higher (28.3%), while that of HPAM was only 17.2%. Thereafter, the utilization sequence of oil during the displacement process was studied with nuclear magnetic resonance experiments. Ultimately, the oil displacement mechanism of HPAM/S-SiQDs was deeply analyzed, including viscosity thickening and wetting reversal.

Assembly of Ultralight Dual Network Graphene Aerogel with Applications for Selective Oil Absorption.

High-performance graphene aerogels with well-developed internal structures are generally obtained by means of introducing additive materials such as carbon nanotubes, cellulose, and lignin into the aerogel network, which not only enhances the cost but also complicates the preparation process. Therefore, tailoring the internal structure of pristine graphene aerogel in a feasible way to achieve high performance is of great significance to the practical applications. Herein, a novel cysteamine/l-ascorbic acid graphene aerogel (CLGA) was fabricated by a simple one-step hydrothermal method followed by freeze-drying. Through the creative combination of the reducing agent l-ascorbic acid and cross-linking agent cysteamine, a dual-network structure was constructed by both layered physical stacking and vertical chemical cross-linking. The addition of cysteamine not only enhanced the reduction degree but also assisted the formation of more vertical connections between graphene nanosheets, resulting in more abundant pores with smaller sizes compared with graphene aerogels prepared by the traditional hydrothermal reduction method. CLGA possessed an ultra-low density of 4.2 mg/cm3 and a high specific surface area of 397.9 m2/g. As expected, this dual-network structure effectively improved the absorption capacity toward a variety of oil and organic solvents, with an outstanding oil absorption capacity up to 310 g/g. Furthermore, CLGA possessed good mechanical properties and oil/water selectivity. The absorbed oil could be recovered by both continuous absorption-removal process and mechanical squeezing, making the as-prepared aerogel superior absorbent material for a variety of applications, such as selective oil absorption and water treatment.

Study on the Reducing Injection Pressure Regulation of Hydrophobic Carbon Nanoparticles.

The interest in the application of nanofluid in reducing injection pressure has been increasing especially for tight reservoirs. In this work, a new type of hydrophobic carbon nanofluid was prepared and the pressure-reducing performance was investigated. The results of particle size distribution, zeta potential, and transmission electron microscopy image showed that the dispersion of nanofluid was uniform and stable. In addition, the hydrophobic carbon nanofluid showed excellent antitemperature and antisalinity property. The contact angle of oil-wet glass slide can range from 45 to 89° after it adsorbs hydrophobic carbon nanoparticles (HCNPs). The atomic force microscope tests showed that the core surface roughness was reduced about 16.67%. The core flooding tests showed that the pressure-reducing rate of 0.15 wt % HCNP nanofluid can reach 17.00%. HCNPs show good performance in reducing pressure and have a broad application prospect in oil field development.

Stability Mechanism of Nitrogen Foam in Porous Media with Silica Nanoparticles Modified by Cationic Surfactants.

This work aims at studying the effect of electrostatic interactions between cationic surfactants and silica nanoparticles (NPs) on foam stability in porous media. The physio-chemical property of NPs, the gas-liquid interface properties, the foam flow characteristics, together with the stability under different concentrations of surfactant and NPs were investigated and compared. It was found that the affinity of silica NPs to the surface is tunable by variation of surfactant concentrations. NPs and surfactants as a whole assembling at the surface substantially improve the foam stability in static and dynamic tests. These surfactant-modified NPs accumulate at the bubble surface and remain stable under dilution of brine, providing a barrier effectively preventing coalescence. In addition, foam stability is enhanced since the layer of NPs significantly reduces the mass transfer rate, consequently mitigating the Ostwald ripening.

The mechanism difference between CO2 and pH stimuli for a dual responsive wormlike micellar system.

To indicate the difference between pH and CO2 stimuli mechanisms, a dual responsive system is constructed with the aid of N-[3-(dimethylamino)propyl]docosanamide (NDPD) and sodium salicylate (NaSal), which is responsive to pH and CO2. The dual responsive system is characterized by rheometry, cryo-TEM and 1H NMR spectroscopy. After bubbling CO2 or adjusting the pH, the rheological properties indicate the formation of wormlike micelles. The cyro-TEM images also confirmed wormlike micelles. The effect of temperature is also clarified. By comparing the rheological properties of the wormlike micelles with pH and CO2 stimuli conditions, combined with cryo-TEM and 1H NMR results, the stimuli mechanisms of pH and CO2 to the dual responsive system are shown. Through this work, we expect to deepen our understanding of the responsiveness of a self-assembled system.

Alternating electric field-induced ion current rectification and electroosmotic pump in ultranarrow charged carbon nanocones.

Pumping fluid in ultranarrow (sub-2 nm) synthetic channels, analogous to protein channels, has widespread applications in nanofluidic devices, molecular separation, and related fields. In this work, molecular dynamics simulations were performed to study a symmetrical sinusoidal electric field-induced electroosmotic pump in ultranarrow charged carbon nanocone (CNC) channels. The results show that the CNC channels could rectify the ion current because of the different ion flow rates in the positive and negative half circles of the sinusoidal electric field. Electroosmotic flow (EOF) rectification yielded by the ion current rectification is also revealed, and net water flow from the base to the tip of the CNC channels is observed. The simulations also show that the preferential ion current conduction direction in the ultranarrow CNC channels (from base to tip) is opposite to that in conical nanochannels with tip diameters larger than 5 nm (from tip to base). However, the preferential EOF direction is the same as that of large conical nanochannels (from base to tip). We also investigated the influences of ion concentration and the amplitudes and periods of the sinusoidal electric field on the EOF pump. The results show that high ion concentration, large amplitudes, and long periods are desired for high EOF pumping efficiency. Finally, through comparison with a constant electric field and a pressure-induced water pump, we prove that the EOF pump under an alternating electric field has a higher pump efficiency. The approach outlined in this work provides a general scheme for pumping fluid in ultranarrow charged conical nanochannels.

Investigation of Novel Triple-Responsive Wormlike Micelles.

Smart wormlike micelles with stimuli-tunable rheological properties may be useful in a variety of applications, such as in molecular devices and sensors. The formation of triplestimuli-responsive systems so far has been a challenging and important issue. In this work, a novel triplestimuli (photo-, pH-, and thermoresponsive) wormlike micelle is constructed with N-cetyl-N-methylmorpholinium bromide and trans-cinnamic acid (CA). The corresponding multiresponsive behaviors of wormlike micellar system were revealed using cryogenic transmission electron microscopy, a rheometer, and 1H NMR. The rheological properties of wormlike micellar system under different temperatures, pH conditions, and UV irradiation times are measured. As confirmed by 1H NMR, chemical structure of a CA molecule can be altered by the multiple stimulation from an exotic environment. We expect it to be a good model for triple-responsive wormlike micelles, which is helpful to understand the mechanism of triple-responsiveness and widen their applications.

A pH-responsive wormlike micellar system of a noncovalent interaction-based surfactant with a tunable molecular structure.

Responsive wormlike micelles are very useful in a number of applications, whereas it is still challenging to create dramatic viscosity changes in wormlike micellar systems. Here we developed a pH-responsive wormlike micellar system based on a noncovalent constructed surfactant, which is formed by the complexation of N-erucamidopropyl-N,N-dimethylamine (UC22AMPM) and citric acid at the molar ratio of 3 : 1 (EACA). The phase behavior, aggregate microstructure and viscoelasticity of EACA solutions were investigated by macroscopic appearance observation, rheological and cryo-TEM measurements. It was found that the phase behavior of EACA solutions undergoes transition from transparent viscoelastic fluids to opalescent solutions and then phase separation with white floaters upon increasing the pH. Upon increasing the pH from 2.03 to 6.17, the viscosity of wormlike micelles in the transparent solutions continuously increased and reached ∼683 000 mPa s at pH 6.17. As the pH was adjusted to 7.31, the opalescent solution shows a water-like flowing behaviour and the η0 rapidly declines to ∼1 mPa s. Thus, dramatic viscosity changes of about 6 magnitudes can be triggered by varying the pH values without any deterioration of the EACA system. This drastic variation in rheological behavior is attributed to the pH dependent interaction between UC22AMPM and citric acid. Furthermore, the dependence on concentration and temperature of the rheological behavior of EACA solutions was also studied to assist in obtaining the desired pH-responsive viscosity changes.

The effect of hydroxyl on the solution behavior of a quaternary ammonium gemini surfactant.

The adsorption and viscoelastic properties of a micellar solution of 2-hydroxyl-propanediyl-1,3-bis(hexadecyldimethylammonium bromide), abbreviated as 16-3OH-16, have been investigated by surface tension and rheological measurements. Meanwhile, an aqueous solution of propanediyl-1,3-bis(hexadecyldimethylammonium bromide), abbreviated as 16-3-16, was also examined. From the steady state and oscillatory rheological results, a notable difference in shear viscosities between the two systems was observed. Zeta potentials and size distributions confirm the change in the potentials and hydrodynamic diameters, and these results are in good agreement with the rheological results. The differences of the two solutions were attributed to the effect of the hydroxyl group on the spacer of 16-3OH-16. Molecular dynamic simulations and density functional theory (DFT) calculations were performed to investigate the non-covalent interactions in the solution and the difference between the molecular orbitals and the electrostatic potentials. Our research shows that a more uniform distribution of positive charges around the spacer could result in a more effective electrostatic screening effect between the charged headgroups, and promote the formation of a worm-like micelle. Also, hyperconjugation becomes stronger when the hydroxyl group is introduced on the spacer of the gemini molecule.

Rheological characterizations and molecular dynamics simulations of self-assembly in an anionic/cationic surfactant mixture.

The formation of self-assemblies in mixed amino acid-based anionic N-hexadecanoylglutamic acid (HGA) and cationic benzyldimethyl hexadecylammonium chloride (HDBAC) surfactants in aqueous solutions has been characterized. With rheological analysis, the viscoelastic properties of the mixed system are found to be completely dependent on the concentration of HDBAC. Molecular dynamics simulation results suggest that the morphology of self-assembly can be regulated from spherical micelles to wormlike micelles by the addition of HDBAC. The aromatic group of HDBAC adsorption provides a "charge-neutral" function to the micelle corona; the repulsive interactions within the head group of HGA are progressively screened and closely packed. In addition, the dynamic processes and formation mechanisms of self-assembly were analyzed in detail with molecular simulation techniques.

Synergistic effect of pH-responsive wormlike micelles based on a simple amphiphile.

Imagine a novel solution that can be switched reversibly from low viscosity to high viscosity with only one additive, upon different commands. To this end, we have developed a simple and effective route to form smart, multi-response wormlike micelles based on a synthesized surfactant, N-cetyl-N,N-diisopropanolammonium bromide (CDIAB). Moreover, we provide new insight into the effects of synergy on this smart wormlike micelle. Rheological measurements were used to study the morphology of the wormlike micelles; (1)H NMR spectroscopy and density functional theory (DFT) calculations were employed to investigate the molecular arrangements and mechanism of the synergy involved in the reversible reactions of pH-response and CO2-response of the micelles in solution. Based on the abovementioned results, it is encouraging to discover that binding energy and electrostatic interaction are the basic driving forces in the formation of wormlike micelles. Moreover, stable viscoelastic behavior was observed in the CDIAB system, with strong binding energy and electrostatic interactions. It is highly anticipated that the synergy observed in this surfactant will be of particular interest due to its novel mechanism and unique properties.

The role of hydroxyethyl groups in the construction of wormlike micelles in the system of quaternary ammonium surfactant and sodium salicylate.

To understand the role of electrostatic interactions and hydrogen bonds in the formation of wormlike micelles with the aid of sodium salicylate, two quaternary ammonium surfactants with the headgroup decorated by one hydroxyethyl group N-cetyl-N-(2-hydroxyethyl)dimethylammonium bromide and two hydroxyethyl groups N-cetyl-N,N-di(2-hydroxyethyl)methylammonium bromide, abbreviated as CHEMAB and CDHAB, respectively, were synthesized in this work. Single crystal X-ray diffraction was used to study the intermolecular interactions of surfactants, and (1)H NMR and rheological measurements were employed to investigate the molecular arrangement and morphology of the wormlike micelles. The synergistic interactions of hydrogen bonding and more effective shielding of electrostatic repulsion contribute to the formation and viscoelastic behavior of wormlike micelles. The results also revealed the aggregation behavior of surfactants with hydroxyethyl headgroups in aqueous solutions.

Aggregation behavior of long-chain piperidinium ionic liquids in ethylammonium nitrate.

Micelles formed by the long-chain piperidinium ionic liquids (ILs) N-alkyl-N-methylpiperidinium bromide of general formula CnPDB (n = 12, 14, 16) in ethylammonium nitrate (EAN) were investigated through surface tension and dissipative particle dynamics (DPD) simulations. Through surface tension measurements, the critical micelle concentration (cmc), the effectiveness of surface tension reduction (Πcmc), the maximum excess surface concentration (Гmax) and the minimum area occupied per surfactant molecule (Amin) can be obtained. A series of thermodynamic parameters (DG0 m, DH0 m and DS0 m) of micellization can be calculated and the results showed that the micellization was entropy-driven. In addition, the DPD simulation was performed to simulate the whole aggregation process behavior to better reveal the micelle formation process.

Universal Approximation Abilities of a Modular Differentiable Neural Network.

Approximation ability is one of the most important topics in the field of neural networks (NNs). Feedforward NNs, activated by rectified linear units and some of their specific smoothed versions, provide universal approximators to convex as well as continuous functions. However, most of these networks are investigated empirically, or their characteristics are analyzed based on specific operation rules. Moreover, an adequate level of interpretability of the networks is missing as well. In this work, we propose a class of new network architecture, built with reusable neural modules (functional blocks), to supply differentiable and interpretable approximators for convex and continuous target functions. Specifically, first, we introduce a concrete model construction mechanism with particular blocks based on differentiable programming and the composition essence of the max operator, extending the scope of existing activation functions. Moreover, explicit block diagrams are provided for a clear understanding of the external architecture and the internal processing mechanism. Subsequently, the approximation behavior of the proposed network to convex functions and continuous functions is rigorously proved as well, by virtue of mathematical induction. Finally, plenty of numerical experiments are conducted on a wide variety of problems, which exhibit the effectiveness and the superiority of the proposed model over some existing ones.

Construction of supramolecular self-assembled microfibers with fluorescent properties through a modified ionic self-assembly (ISA) strategy.

Highly ordered supramolecular microfibers were constructed through a simple ionic self-assembly strategy from complexes of the N-tetradecyl-N-methylpyrrolidinium bromide (C(14)MPB) surface-active ionic liquid and the small methyl orange (MO) dye molecule, with the aid of patent blue VF sodium salt. By using scanning electron microscopy and polarized optical microscopy, the width of these self-assembled microfibers is observed to be about 1 to 5 µm and their length is from tens of micrometers to almost a millimeter. The (1)H NMR spectra of the microfibers indicates that the supramolecular complexes are composed of C(14)MPB and MO in equal molar ratio. The electrostatic, hydrophobic, and π-π stacking interactions are regarded as the main driving forces for the formation of microfibers. Furthermore, through characterization by using confocal fluorescence microscopy, the microfibers were observed to show strong fluorescent properties and may find potential applications in many fields.

Recent advances in enhanced polymer gels for profile control and water shutoff: A review.

Polymer gels have been effectively employed as a water management material for profile control and water shutoff treatments in low-middle temperature and low-middle salinity reservoirs. However, most polymer gel systems have limitations under high temperature and salinity reservoir conditions, such as short gelation time, poor strength, and long-term instability. Therefore, several researchers have developed enhanced polymer gels to satisfy the water control requirements in high temperature and salinity reservoirs. This work reviews the five main types of enhanced polymer gels that have been developed so far: nano silica-enhanced gel systems, cellulose-enhanced gel systems, graphite-enhanced gel systems, oily sludge-enhanced gel systems, and foam-enhanced polymer gel systems. Further, this article investigates the fundamental properties, strengthening and crosslinking mechanisms, reservoir application conditions, and field applications of several enhanced polymer systems. In this paper, it is found that the addition of strengthening materials can increase the bound water content in the gel network and significantly improve the temperature and salt resistance of polymer gel, so as to cope with the application of profile control and water plugging in high temperature and high salt reservoirs. Moreover, it also offers references and future research directions for enhanced polymer gel systems.

Development and Gelation Mechanism of Ultra-High-Temperature-Resistant Polymer Gel.

To expand the applicability of gel fracturing fluids in ultra-high-temperature reservoirs, a temperature-resistant polymer was synthesized using the solution polymerization method. Subsequently, an ultra-high-temperature-resistant polymer gel was formulated by incorporating an organic zirconium crosslinking agent. A comprehensive investigation was carried out to systematically study and evaluate the steady shear property, dynamic viscoelasticity, and temperature and shear resistance performance, as well as the core damage characteristics of the polymer gel. The obtained results demonstrate that the viscosity remained at 147 mPa·s at a temperature of 200 °C with a shear rate of 170 s-1. Compared with the significant 30.9% average core damage rate observed in the guanidine gum fracturing fluid, the core damage attributed to the polymer gel was substantially mitigated, measuring only 16.6%. Finally, the gelation mechanism of the polymer gel was scrutinized in conjunction with microscopic morphology analysis. We expect that this study will not only contribute to the effective development of deep and ultradeep oil and gas reservoirs but also furnish a theoretical foundation for practical field applications.

A Supramolecular Reinforced Gel Fracturing Fluid with Low Permeability Damage Applied in Deep Reservoir Hydraulic Fracturing.

Gel fracturing fluid is the optimum fracturing fluid for proppant suspension, which is commonly applied in deep reservoir hydraulic fracturing. The content of polymers and crosslinkers in gel fracturing fluid is usually high to meet the needs of high-temperature resistance, leading to high costs and reservoir permeability damage caused by incomplete gel-breaking. In this paper, a supramolecular reinforced gel (SRG) fracturing fluid was constructed by strengthening the supramolecular force between polymers. Compared with single network gel (SNG) fracturing fluid, SRG fracturing fluid could possess high elasticity modulus (G' = 12.20 Pa) at lower polymer (0.4 wt%) and crosslinker (0.1 wt%) concentrations. The final viscosity of SRG fracturing fluid was 72.35 mPa·s, meeting the temperature resistance requirement of gel fracturing fluid at 200 °C. The gel-breaking time could be extended to 90-120 min using an encapsulated gel breaker. Gel particles are formed after the gel fracturing fluid is broken. The median particle size of gel particles in the SRG-breaking solution was 126 nm, which was much smaller than that in the industrial gel (IDG) breaking fluid (587 nm). The damage of the SRG-breaking solution to the core permeability was much less than the IDG-breaking solution. The permeability damage of cores caused by the SRG-breaking solutions was only about half that of IDG-breaking solutions at 1 mD.

Novel Anionic-Nonionic Surfactant Based on Water-Solid Interfacial Wettability Control for Residual Oil Development.

Irreversible colloidal asphaltene adsorption layers are formed on formation rock surfaces due to long-term contact with crude oil, and large amounts of crude oil adhere to these oil-wet layers to form residual oil films. This oil film is difficult to peel off due to the strong oil-solid interface effect, which seriously restricts further improvement in oil recovery. In this paper, the novel anionic-nonionic surfactant sodium laurate ethanolamide sulfonate (HLDEA) exhibiting strong wetting control was synthesized by introducing sulfonic acid groups into the nonionic surfactant laurate diethanolamide (LDEA) molecule through the Williamson etherification reaction. The introduction of the sulfonic acid groups greatly improved the salt tolerance and the absolute value of the zeta potential of the sand particles. The experimental results showed that HLDEA altered the wettability of the rock surface from oleophilic to strongly hydrophilic, and the underwater contact angle increased substantially from 54.7 to 155.9°. In addition, compared with LDEA, HLDEA exhibited excellent salt tolerance and enhanced oil recovery performance (the oil recovery was improved by 19.24% at 2.6 × 104 mg/L salinity). Based on nanomechanical experimental results, HLDEA was efficiently adsorbed on the core surfaces and regulated microwetting. Moreover, HLDEA effectively reduced the adhesion force between the alkane chains and the core surface, which facilitated residual oil stripping and oil displacement. This new anionic-nonionic surfactant affording great oil-solid interface wetting control has practical significance for the efficient development of residual oil.

Probing the Effect of Young's Modulus on the Reservoir Regulation Abilities of Dispersed Particle Gels.

The mechanical strength of dispersed particle gels (DPGs), which can be directly characterized by Young's modulus, is an important parameter affecting reservoir regulation performance. However, the effect of reservoir conditions on the mechanical strength of DPGs, as well as the desired range of mechanical strength for optimum reservoir regulation performance, have not been systematically studied. In this paper, DPG particles with different Young's moduli were prepared and their corresponding migration performances, profile control capacities and enhanced oil recovery abilities were studied by simulated core experiments. The results showed that with increase in Young's modulus, the DPG particles exhibited improved performance in profile control as well as enhanced oil recovery. However, only the DPG particles with a modulus range of 0.19-0.762 kPa could achieve both adequate blockage in large pore throats and migration to deep reservoirs through deformation. Considering the material costs, applying DPG particles with moduli within the range of 0.19-0.297 kPa (polymer concentration: 0.25-0.4%; cross-linker concentration: 0.7-0.9%) would ensure optimum reservoir control performance. Direct evidence for the temperature and salt resistance of DPG particles was also obtained. When aged in reservoir conditions below 100 °C and at a salinity of 10 × 104 mg·L-1, the Young's modulus values of the DPG particle systems increased moderately with temperature or salinity, indicating a favorable impact of reservoir conditions on the reservoir regulation abilities of DPG particles. The studies in this paper indicated that the practical reservoir regulation performances of DPGs can be improved by adjusting the mechanical strength, providing basic theoretical guidance for the application of DPGs in efficient oilfield development.