Decrease In Interfacial Tension Research Articles

Effect of Alkyl Peroxyl Radical Oxidation on the Oxidative Stability of Walnut Protein Emulsions and Their Adsorbed Proteins

Walnuts are high in protein content and rich in nutrients and are susceptible to oxidation during production and processing, leading to a decrease in the stability of walnut protein emulsions. In this paper, the effect of alkyl peroxyl radical oxidation on the stability of walnut protein emulsions is investigated. With the increase of 2,2-azobis (2-methylpropionamidine) dihydrochloride (AAPH) concentration, both its protein and fat were oxidized to different degrees, and the droplets of the emulsion were first dispersed and then aggregated as seen from the laser confocal, and the stability of walnut protein emulsion was best at the AAPH concentration of 0.2 mmol/L. In addition to this, the adsorption rate of adsorbed proteins showed a decreasing and then an increasing trend with the increase in the oxidized concentration. The results showed that moderate oxidation (AAPH concentration: 0–0.2 mmol/L) promoted an increase in protein flexibility and a decrease in the protein interfacial tension, leading to the decrease in emulsion droplet size and the increase of walnut protein emulsion stability, and excessive oxidation (AAPH concentration: 1–25 mmmol/L) weakened protein flexibility and electrostatic repulsion, making the walnut protein emulsion less stable. The results of this study provide theoretical references for the quality control of walnut protein emulsions.

Investigation of the processes of additional oil displacement by nanosuspension silicon oxide from a model core

The use of nanosuspensions during reservoir flooding is an alternative to chemical methods for enhancing oil recovery. In this work, the effectiveness of using nanosuspensions as a post-displacement agent after the base agent (water) was shown. Filtration tests for additional oil displacement from model rock samples were carried out. Suspensions of nanoparticles were used for post-displacement. The mass concentration of spherical silicon oxide nanoparticles (SiO2) varied from 0.01 to 0.25%wt, and their size varied from 10 to 35 nm. The permeability of the model core was 50 mD. An experimental measurement of the interfacial tension and the contact angle of wettability was performed. It is shown that with an increase in the concentration of nanoparticles, the interfacial tension of the “oil — suspension” decreases. It has been established that at a fixed concentration of nanoparticles (0.1%), with an increase in the size of nanoparticles, the interfacial tension decreases. It was revealed that when using suspensions, the contact angle of rock wetting with oil changes significantly. As a result of filtration tests, dependences of the oil displacement efficiency on the concentration and size of nanoparticles were obtained. It has been shown that additional volume of oil can be recovered after filtering nanosuspensions.

Advanced machine learning-based modeling of interfacial tension in the crude oil-brine-diethyl ether system: Insights into the effects of temperature and salinity

Solvent injection, a well-established method for enhanced oil recovery (EOR), has demonstrated significant improvements in oil recovery when compared with conventional water flooding techniques. The interfacial tension (IFT) is pivotal in determining the displacement efficiency and overall performance of innovative techniques like dimethyl ether-enhanced waterflooding (DEW), which has gained substantial attention in recent years. In this study, following laboratory measurements of IFT, six advanced machine learning (ML) techniques were employed: Generalized Linear Model (GLM), Gradient Additive Model (GAM), Random Forest (RF), Support Vector Machine (SVM), Extreme Gradient Boosting (XGBoost), and Boosted Regression Tree (BRT) to model the IFT in both oil-brine and oil-brine-diethyl ether (DEE) systems. The analysis is based on an extensive dataset comprising 7,017 data points for oil-brine and 6,949 data points for oil-brine-DEE systems obtained from experimental studies. The findings indicate that the developed RF model excels in predicting IFT, boasting a remarkable coefficient of determination (R2 = 0.99) along with the lowest root mean squared error (RMSE = 0.2), mean squared error (MSE = 0.04), and mean absolute error (MAE = 0.13). The study underscores the significance of optimizing salinity levels to achieve the most substantial reduction in IFT. This reduction is attributed to the enhanced migration of polar components, such as asphaltene molecules, to the interface of the oil-brine system. Moreover, the research highlights a synergistic decrease in IFT when both DEE and soluble ions are present, resulting in the lowest IFT at around 2 mN/m in 40,000 ppm salinity (S2) at 70 °C (T3). This indicates that the adsorption of DEE at the water–oil interface forms a layer capable of adsorbing ions, thereby enhancing the layer's thickness. As a result, the oil–solvent-ion layer becomes thicker compared to the oil-ion layer, leading to the maximum decrease in IFT. Additionally, with increasing temperature up to 70 °C, the IFT of both systems demonstrated a downward trend, as evidenced by all experiments. The outcomes of this study have the potential to enhance our comprehension of the underlying mechanisms involved in water-soluble solvent EOR techniques.

Probing Effect of 6MeV Electron Beam Irradiation on Haemoglobin Protein Using Spectroscopic Techniques.

In this work, we study the effect of 6MeV electron beam irradiation on the physicochemical properties of lyophilized Human Haemoglobin A (HbA). Electron beams generated from Race Track Microtron accelerator with energy 6MeV were used to irradiate HbA at fluences of 5 × 1014 e-/cm2 and 10 × 1014 e-/cm2. Pristine and electron beam irradiated HbA were characterized using UV-visible and Fourier transform infrared spectroscopy (FTIR) spectroscopy. The interfacial tension of the aqueous solutions of HbA are also analysed by pendant drop method. Absorbance intensity, % transmittance and interfacial tension decrease with fluence. The peak position of the Soret band (λsoret = 404nm) remains unaffected by the fluences. FTIR spectroscopy confirms the changes in the secondary structure of the haemoglobin. In the amide band I, the percentage of α-helix reduced from 8% to 1%, and an increase in β-sheet (19% to 29%) and β helix (6.3% to 15%) is observed. Interfacial tension decreases from 46.0mN/m and 44.0mN/m with increase in irradiation dose. These finding provides realistic guideline for biological cells exposure to electron beam radiation doses.

Exploring the Effect of Relaxation Time, Natural Surfactant, and Potential Determining Ions (Ca2+, Mg2+, and SO42−) on the Dynamic Interfacial Tension Behavior of Model Oil-Brine Systems

This study examined how the concentration of asphaltene and divalent ions in various salinities affects the interfacial tension (IFT) between a model oil/brine using the pendant drop method. The oleic phase consisted of a mixture of toluene and n-heptane (heptol), to which asphaltene was added to investigate how asphaltene molecules affect the surface properties. The base fluid was prepared with a salinity of 40,000 ppm, and two additional solutions with concentrations of 4000 ppm (low salinity) and 80,000 ppm (high salinity) were created. The results revealed that increasing the concentration of asphaltene within certain salinity ranges led to a decrease in IFT. The lowest IFT was observed at the 40,000 ppm salinity level, indicating that at this optimal salinity, the maximum asphaltene concentration migrated to the heptol/brine interface, reducing the IFT from 23 mN/m to 16 mN/m. Additionally, a 0.5 % wt of asphaltene demonstrated a significant concentration of micellization of natural surfactants, suggesting that the interface was nearly saturated with asphaltene. Consequently, concentrations higher than this value did not significantly alter the IFT. In the final part of the study, the impact of divalent ions was investigated, revealing that as the concentration of Ca2+ ions increased up to fourfold, the IFT decreased to 15 mN/m, about 10 % less than the base case. This value represented the lowest IFT compared to Mg2+ and SO42−. Moreover, modeling the results indicated that the relaxation time decreased with increasing salinity, suggesting that higher salinity accelerated the process of asphaltene absorption at the interface.

Effect of type of fatty acid attached to sucrose ester on the stability of water-in-oil Pickering emulsion

Water-in-oil (W/O) Pickering emulsions have a broad range of potential for use in the food industries. However, because of the scarcity of edible W/O-type particles, the production and stabilization of W/O Pickering emulsion is challenged. Sucrose esters (SEs) have great promise as W/O-type particles, whose properties vary with fatty acid moiety attached. This study investigated the effect of fatty acid residue type on the interface activity of SE and corresponding emulsion properties, in order to select the most suitable SE. Sucrose stearate (SE-S), sucrose palmitate (SE-P), sucrose laurate (SE-L), sucrose erucic acid ester (SE-E) and sucrose oleate (SE-O) were applied. Results showed that the saturation of fatty acid residues caused the difference of crystallinity of SE: SE-S＞SE-P＞SE-L＞SE-E＞SE-O. The lower crystallinity resulted in the increased hydrophilicity of SE-O with a closer θ (101.4°) to 90°, which facilitated interfacial adsorption and rearrangement, and larger decrease of interfacial tension (3.93 mN/m). Consequently, SE-O was capable of stabilizing more water volume fraction (75%). Moreover, the emulsion stabilized by SE-O was observed smaller droplet sizes, higher gel strength, and physical stability. The results revealed that SE-O was more appropriate for the preparation of W/O Pickering emulsion.

Effect of ionic environment in aqueous solution on nucleation and stabilization of bulk nanobubbles

Bulk nanobubbles have attracted significant interest due to their growing demand for widespread applications. A thorough comprehension of the essential factors dictating nanobubble properties holds immense significance in industrial practices. This study endeavors to examine the characteristics of bulk nanobubbles formed in a complex ionic solution containing surfactants and sodium chloride. The experimental findings demonstrate that both ionic and nonionic surfactants can effectively promote the nucleation of nanobubbles. The introduction of salts has an opposing effect as it reduces both the number concentration and the Zeta potential of nanobubbles. There is a concentration threshold for NaCl above which the nanobubble properties are significantly affected. The salt effectively promotes the adsorption of surfactant ions, which in turn leads to a decrease in interfacial tension. The Zeta potential of nanobubbles is established through the competing interactions between the surface adsorption and ion shielding effect. Subsequently, the critical stable conditions for nanobubbles generated in solutions containing surfactants and salts are calculated, while considering both the kinetic stability of nanobubble populations and the thermodynamic stability of individual nanobubbles. These findings offer valuable insights into the intricate influence of complex aqueous ionic environment on nanobubbles, thereby setting the stage for the deliberate manipulation of them.

A Feasibility Study on Enhanced Oil Recovery of Modified Janus Nano Calcium Carbonate-Assisted Alkyl Polyglycoside to Form Nanofluids in Emulsification Flooding.

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.

Reversible phase separation of CO2 responsive microemulsion: Judgment on whether and how regulated by ratio of ion to responsive surfactant concentration

CO2 responsive microemulsion is a promising solvent with diverse applications in various fields including oil exploitation, material synthesis, and metal recovery. The implementation of reversible phase separation becomes important in enabling the reuses of CO2 responsive microemulsion and facilitating the separation of products in these applications. Earlier reports have established that changes in ion concentration within CO2 responsive microemulsion result in reversible phase separation. Ion in CO2 responsive microemulsion is derived from protonation of CO2 responsive substance which is commonly used as surfactant. An increase in ion concentration leads to a decrease in surfactant concentration. In microemulsion, adsorption of surfactants and ions at the oil–water interface is correlated with interface performance, which influence the ability to achieve efficient phase separation. Interfacial tension (IFT) is an important parameter for interface performance. In this work, ratio of ion to CO2 responsive surfactant concentration was defined as ∮. The relationship between IFT and ∮ was investigated through a combination of experiments and molecular dynamic simulation to explore mechanism of reversible phase separation. The results of present study indicated that ∮ was found to play a vital role in either inhibiting or promoting the formation of hydrogen bond network by hydrophilic groups in surfactants. The changes of hydrogen bond network resulted in increase or decrease in IFT, leading to reversible phase separation. This relationship between IFT and ∮ was used as a theoretical guidance to optimize N2/CO2 bubbling time to achieve reversible phase separation. The optimization improved the efficiency of CO2 responsive microemulsion in extracting active components from Rehmannia glutinosa Libosch. leaves, and enhanced sustainability of the microemulsion. The findings of this study could be used to advance the scientific understanding of reversible phase separation, offering theoretical guidance for green and efficient utilization of CO2 responsive microemulsion in extraction of natural products. Ultimately these results could encourage the broader applications of CO2 responsive microemulsion across diverse fields.

Interfacial Tension Hysteresis of Eutectic Gallium‐Indium

AbstractWhen in a pristine state, gallium and its alloys have the largest interfacial tensions of any liquid at room temperature. Nonetheless, applying as little as 0.8 V of electric potential across eutectic gallium indium (EGaIn) placed within aqueous sodium hydroxide (NaOH, or other electrolyte) solution will cause the metal to behave as if its interfacial tension is near zero. The mechanism behind this phenomenon has remained poorly understood because NaOH dissolves the oxide species, making it difficult to directly measure the concentration, thickness, or chemical composition of the film that forms at the interface. In addition, the oxide layers formed are atomically‐thin. Here, it presents a suite of techniques that allow to simultaneously measure both electrical and interfacial properties as a function of applied electric potential, allowing for new insights into the mechanisms, which cause the dramatic decrease in interfacial tension. A key discovery from this work is that the interfacial tension displays hysteresis while lowering the applied potential. It combines these observations with electrochemical impedance spectroscopy to evaluate how these changes in interfacial tension arise from chemical, electrical, and mechanical changes on the interface, and close with ideas for how to build a free energy model to predict these changes from first principles.

Ultrasound-Induced Adsorption of Acousto-Responsive Microgels at Water-Oil Interface.

Ultrasonic mixing is a well-established method to disperse and mix substances. However, the effects of ultrasound on dispersed soft particles as well as on their adsorption kinetics at interfaces remain unexplored. Ultrasound not only accelerates the movement of particles via acoustic streaming, but recent research indicates that it can also manipulate the interaction of soft particles with the surrounding liquid. In this study, it evaluates the adsorption kinetics of microgel at the water-oil interface under the influence of ultrasound. It quantifies how acoustic streaming accelerates the reduction of interfacial tension. It uses high-frequency and low-amplitude ultrasound, which has no destructive effects. Furthermore, it discusses the ultrasound-induced shrinking and thus interfacial rearrangement of the microgels, which plays a secondary but non-negligible role on interfacial tension reduction. It shows that the decrease in interfacial tension due to the acoustic streaming is stronger for microgels with higher cross-linker density. Moreover, it shows that ultrasound can induce a reversible decrease in interfacial tension due to the shrinkage of microgels at the interface. The presented results may lead to a better understanding in any field where ultrasonic waves meet soft particles, e.g., controlled destabilization in foams and emulsions or systems for drugrelease.

Interfacial adsorption of soybean phosphatidylethanolamine in different oil phase and the stability of water-in-oil emulsion

Water-in-oil (W/O) emulsion holds great potential in designing fat-reduced foods. However, due to the lack of W/O-type surfactant, formation of all-natural W/O emulsion is challenged. This study aimed to investigate the effect of oil phase on interfacial adsorption of soybean phosphatidylethanolamine (SP) and stability of W/O emulsion. Five oils, including medium chain triglycerides oil (MO), coconut oil (CO), palm kernel oil (PKO), sunflower oil (SO) and rapeseed oil (RO), were selected. Results showed that diffusion rate of SP to the interface ranked as MO > CO > PKO > SO ≈ RO, increasing interfacial adsorption from 50.2 % to 85.3 %. Higher interfacial adsorption improved the deformation resistance of interfacial layer, causing more significant decrease in interfacial tension (3.54 mN/m). So, the largest water fraction (65 %) was stabilized by SP with MO and CO, and exhibited smaller droplet sizes and better stability. Consequently, shorter-chain oil was more suitable for preparing W/O emulsions.

A numerical study on the effect of wall wettability on film formation in liquid–liquid slug flow

This study numerically investigates the effect of the contact angle on the hydrodynamics of liquid–liquid slug flow in a capillary with an internal diameter of 2.4 mm. The finite volume method is used to solve the Navier–Stokes equation, and the volume-of-fluid method is employed for interface capturing. The contact angle varies from 13° to 169°. The aqueous phase is observed as a continuous medium, the organic phase is in a dispersed phase at low contact angles, and the aqueous phase is dispersed as a medium at high contact angles. The slug velocity is lower at partial wetting contact angles than at fully wetting or non-wetting contact angles. The vorticity inside the slug is higher at extreme contact angles (169°/13°) and becomes very pronounced near the interface. At the Weber number Weslug>0.135, fully developed film is observed. The thickness of this film increases as the interfacial tension decreases. Additionally, the pressure within the slug rises with an increase in interfacial tension.

Biosourced Multiphase Systems Based on Poly(Lactic Acid) and Polyamide 11 from Blends to Multi-Micro/Nanolayer Polymers Fabricated with Forced-Assembly Multilayer Coextrusion

The objective of the present study was to investigate multiphase systems based on polylactic acid (PLA) and polyamide 11 (PA11) from blends to multilayers. Firstly, PLA/PA11 blends compatibilized with a multifunctionalized epoxide, Joncryl, were obtained through reactive extrusion, and the thermal, morphological, rheological, and mechanical behaviors of these materials were investigated. The role of Joncryl as a compatibilizer for the PLA/PA11 system was demonstrated by the significant decrease in particle size and interfacial tension as well as by the tensile properties exhibiting a ductile behavior. Based on these findings, we were able to further clarify the effects of interdiffusion and diffuse interphase formation on the structure, rheology, and mechanics of compatible multilayered systems fabricated with forced-assembly multilayer coextrusion. The results presented herein aim to provide a deeper understanding of the interfacial properties, including the rheological, mechanical, and morphological behaviors, towards the control of the interface and confinement in multilayer polymers resulting from coextrusion, and also to permit their use in advanced applications.

Effect of hydrolyzed polyacrylamide on oil droplet stability in polymer-flooding produced water: variation of oil droplets diameter and oil–water interfacial properties

Hydrolyzed polyacrylamide (HPAM) in polymer flooding leads to stable oil-in-water emulsions, making the oil removal from polymer-flooding produced water (PFPW) more difficult. To elucidate HPAM’s effects on the oil separation performance of conventional physical separation process for PFPW, the stability, and diameter of oil droplets of simulated PFPW were accurately determined using the Turbiscan LAB expert. The results demonstrated that an increase in HPAM’s molecular weight and concentration led to a significant decrease in the diameter of oil droplets in simulated PFPW. When the molecular weight of HPAM increased from 6 to 18 MDa, there was a decrease in the Turbidity Scanning Index (TSI) values from 22.5 to 8.7, along with a significant decline in the diameter of oil droplets from 72.7 to 32.6 µm after a settling period of 40 min. Furthermore, a rise in HPAM concentration inhibited the enlargement of oil droplets. As HPAM concentration increased from 0 to 500 mg/L, the diameter of the oil droplets reduced by 42.1 µm after a 40 min settling period. HPAM's effect on restricting the growth of oil droplets remained relatively constant across oil concentrations ranging from 500 to 2500 mg/L. Moreover, increasing the molecular weight of HPAM from 6 to 18 MDa led to a 41.6% increase in PFPW's viscosity and a 38.9% decrease in oil-water interfacial tension, thereby inhibiting oil droplet coalescence. Our findings provide valuable fundamental guidance for the design of innovative separation methods for PFPW treatment.

Synergistic Interaction of Hyperbranched Polyglycerols and Cetyltrimethylammonium Bromide for Oil/Water Interfacial Tension Reduction: A Molecular Dynamics Study.

Applying surfactants to reduce the interfacial tension (IFT) on water/oil interfaces is a proven technique. The search for new surfactants and delivery strategies is an ongoing research area with applications in many fields such as drug delivery through nanoemulsions and enhanced oil recovery. Experimentally, the combination of hyperbranched polyglycerol (HPG) with cetyltrimethylammonium bromide (CTAB) substantially reduced the observed IFT of oil/water interface, 0.9 mN/m, while HPG alone was 5.80 mN/m and CTAB alone IFT was 8.08 mN/m. Previous simulations in an aqueous solution showed that HPG is a surfactant carrier. Complementarily, in this work, we performed classical molecular dynamics simulations on combinations of CTAB and HPG with one aliphatic chain to investigate further the interaction of this pair in oil interfaces and propose the mechanism of IFT decrease. Basically, from our results, one can observe that the IFT reduction comes from a combination of effects that have not been observed for other dual systems: (i) Due to the CTAB-HPG strong interaction, a weakening of their specific and isolated interactions with the water and oil phases occurs. (ii) Aggregates enlarge the interfacial area, turning it into a less ordered interface. (iii) The spread of individual molecules charge profiles leads to the much lower interfacial tension observed with the CTAB+HPG systems.

Anionic-nonionic and nonionic mixed surfactant systems for oil displacement: Impact of ethoxylate chain lengths on the synergistic effect

Compound surfactant system has been extensively studied in enhanced oil recovery (EOR) as the synergistic effect of mixed surfactants can increase the density of surfactants distributed at the oil/water interface, enhancing the interfacial activity and decreasing the interfacial tension. The system can further increase the capillary number and enhance oil recovery for oil-wet reservoirs. Studying the interactions between surfactant molecules is of great significance to the enhancement of practical application performances. In this study, N, N-dihydroxyethyl alkyl amide (CDEA), and Alkylphenol polyoxyethylene carboxylate (APEC) with different EO numbers were mixed to prepare a binary compound oil displacement system. The influence of the EO number on the synergistic effect of the CDEA/APEC system and the EOR potential was measured by interfacial tension, nanomechanical tests and oil-displacement experiments. The results indicate a synergistic effect between CDEA and APEC due to the formation of hydrogen bonds between the hydroxyl groups of CDEA and the EO chains of APEC. An optimal synergistic effect in the system was obtained when the EO number was four. The CDEA/APEC-4 system exhibited an oil/water interfacial tension decrease to 10−2 mN/m at 75 °C and the oil recovery was 57.14 %, which was increased by 19.2 % compared to primary water flooding. However, a longer EO chain length weakened the interaction forces between CDEA and APEC, which diminished the synergistic effect of the system, leading to an increase of the interfacial tension. Due to the flexibility of the EO chain, the increase in the EO number leads to the bending of APEC molecules. The longer EO chain length weakened the interaction forces between CDEA and APEC, which diminished the synergistic effect of the system, leading to an increase of the interfacial tension. The oil-displacement experiment revealed that the EO chains changed the oil recovery and injection pressure by affecting the interfacial tension of the mixed system. This study has significant implications for the formulation design and optimization of agents for oilfield development.

Characterization of the effects of wettability and pore pressure on the interfacial behavior of CO2 interacting with oil-water two-phase on pore walls

To date, research studies on film-like residual oil have mainly focused on reservoirs in the late stage of water flooding development. However, there have been relatively few studies on film-like residual oil on pore walls after gas flooding. In this study, a molecular dynamics simulation method was used to investigate the behavior characteristics of fluid-fluid and fluid-solid interfaces and the exploitation potential of film-like remaining oil in water-wet, mixed-wet and oil-wet systems under different pore pressures after CO2 flooding. The results indicated that in the oil-in-water system, the cohesive energy density (CED) of the water films was much greater than that of the CO2 and decane components, and the CED of water films in the water-wet systems was slightly greater than the CED of water films in the mixed-wet systems. Regardless of the water-wet or mixed-wet systems, Einter(CO2−decane) was the strongest between the components. Therefore, CO2 molecules could easily enter the oil films and divide the oil phase into clusters of different sizes. The interfacial tension at the CO2 + decane/H2O and H2O/SiO2 interfaces in both the water-wet and mixed-wet systems decreased with increasing pressure. Under the same pressure, the degree of decrease in interfacial tension at the CO2 + decane/H2O interface in the mixed-wet systems was smaller than that in the water-wet systems. The degree of decrease in interfacial tension at the H2O/SiO2 interfaces in the mixed-wet systems was generally greater than that in the water-wet systems. In the water-in-oil system, because the water films isolated the oil films from the CO2 molecules, the interaction energy between the CO2 molecules and oil phase was weak, so the oil films remained on the quartz surfaces. Due to the existence of the hydrogen bond network inside the water phase, the morphological changes in water films were also small when the CO2 molecules interacted with the water phase. At the CO2/H2O interfaces, under the same pressure, the resistance of CO2 molecules to pass through the water films in the oil-wet systems was greater than that in the mixed-wet systems, and the CO2 molecules in the mixed-wet systems were more likely to enter into the water films. The interfacial tension reduction at the interfaces in the mixed-wet systems was smaller than that in the oil-wet systems. At the H2O/decane interfaces, the power of CO2 molecules breaking through the oil-water interfaces and entering into the oil phase in both the mixed-wet and oil-wet systems was basically equal under the same pressure. The interfacial tension reduction at the interfaces in the mixed-wet systems was almost equal to that of the oil-wet systems. At the decane/SiO2 interfaces, the CED of the oil films in the oil-wet systems was greater than that in the oil-wet systems under the same pressures, and the Einter(CO2−SiO2) in the mixed-wet systems was greater than the Einter(CO2−SiO2) in the oil-wet systems, indicating that CO2 molecules were more easily adsorbed on the quartz surfaces in the mixed-wet systems, and the interfacial tension reduction at the interfaces in the mixed-wet systems was greater than that of the oil-wet systems. The interfacial tension at the CO2/H2O, H2O/decane and decane/SiO2 interfaces in both the mixed-wet and oil-wet systems decreased with increasing pressure. The research results provide a reference for understanding the fluid-fluid and fluid-solid interface behaviors and the exploitation potential of film-like residual oil during CO2 gas flooding.

Designing effective enhanced oil recovery fluid: Combination of graphene oxide, D118 SuperPusher, and Chuback surfactant

Enhanced oil recovery (EOR) is one of the most essential branches of petroleum engineering and aims to maximize oil extraction from reservoirs. This research focuses on the utilization of graphene oxide (GO) in combination with a D118 SuperPusher compound and a natural surfactant (Chuback) to enhance oil recovery. The objective is to optimize the efficiency of the EOR process through a multi-component approach. The application of Chuback leads to a substantial decrease in interfacial tension (IFT), particularly in carbonate rock formations. This is attributed to the unique characteristics of carbonate rocks, which exhibit greater susceptibility to wettability alterations. Moreover, GO nanoparticles (NPs) were synthesized, then characterized and incorporated into the surfactant-polymer system, creating surfactant-polymer-nanoparticle (SPN) fluids. The selection of optimum fluid formulations for the EOR process is facilitated through the utilization of Design Expert, a statistical software tool. Factors such as surfactant concentration, polymer concentration, NPs concentration, and two types of salt concentrations are specifically chosen as variables that can influence the fluid's performance during the flooding step. Parameters including IFT, contact angle (CA) (which affects wetting behavior), and shear viscosity (which impacts fluid flow) are considered responses. The efficacy of the suggested fluid formulation for EOR is validated through core flooding investigations. Core flooding investigations validated the efficacy of the suggested fluid for EOR, with recovery factors of up to 30% and 56% in sandstone and carbonate core samples, respectively. These findings underscore the potential of the proposed approach to significantly enhance oil recovery from both sandstone and carbonate reservoirs.

Interfacial Tension-Temperature-Pressure-Salinity Relationship for the Hydrogen-Brine System under Reservoir Conditions: Integration of Molecular Dynamics and Machine Learning.

Hydrogen (H2) underground storage has attracted considerable attention as a potentially efficient strategy for the large-scale storage of H2. Nevertheless, successful execution and long-term storage and withdrawal of H2 necessitate a thorough understanding of the physical and chemical properties of H2 in contact with the resident fluids. As capillary forces control H2 migration and trapping in a subsurface environment, quantifying the interfacial tension (IFT) between H2 and the resident fluids in the subsurface is important. In this study, molecular dynamics (MD) simulation was employed to develop a data set for the IFT of H2-brine systems under a wide range of thermodynamic conditions (298-373 K temperatures and 1-30 MPa pressures) and NaCl salinities (0-5.02 mol·kg-1). For the first time to our knowledge, a comprehensive assessment was carried out to introduce the most accurate force field combination for H2-brine systems in predicting interfacial properties with an absolute relative deviation (ARD) of less than 3% compared with the experimental data. In addition, the effect of the cation type was investigated for brines containing NaCl, KCl, CaCl2, and MgCl2. Our results show that H2-brine IFT decreases with increasing temperature under any pressure condition, while higher NaCl salinity increases the IFT. A slight decrease in IFT occurs when the pressure increases. Under the impact of cation type, Ca2+ can increase IFT values more than others, i.e., up to 12% with respect to KCl. In the last step, the predicted IFT data set was used to provide a reliable correlation using machine learning (ML). Three white-box ML approaches of the group method of data handling (GMDH), gene expression programming (GEP), and genetic programming (GP) were applied. GP demonstrates the most accurate correlation with a coefficient of determination (R2) and absolute average relative deviation (AARD) of 0.9783 and 0.9767%, respectively.