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Low-Salinity Water Flooding (LSWF) is a technique aimed at modifying the interactions between rock and fluids particularly altering wettability and reducing interfacial tension (IFT). However, there remains limited understanding of how heterogeneous wettability and the presence of Initial Water Saturation (Swi) can impact the effectiveness of LSWF. This study contributes to a deeper understanding of LSWF mechanisms in the context of heterogeneous wettability, while also considering Swi. The simulations were conducted using OpenFOAM, employing a non-reactive quasi-three-phase flow solver that accounts for wettability alteration and IFT reduction during the mixing of Low-Salinity (LSW) and High-Salinity Water (HSW). A heterogeneous pore geometry is designed, and four distinct scenarios are simulated, encompassing both heterogeneous and homogeneous wettability conditions while considering the presence of Swi. These scenarios included secondary High-Salinity Water Flooding (HSWF), tertiary and secondary LSWF. Notably, the simulations reveal that secondary LSWF consistently yields the highest oil recovery across all scenarios, achieving recovery rates of up to 96.98 %. Furthermore, the presence of Swi significantly influences the performance of LSWF in terms of oil recovery, particularly in heterogeneous wettability conditions where it boosts recovery by up to 3.5 %, but in homogeneous wettability, it decreases recovery by nearly 26 %. These simulations also underscore the pivotal role played by the distribution of oil and HSW phases in profoundly affecting the outcomes of LSWF.

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The storage of CO2 and hydrogen within depleted gas and oil reservoirs holds immense potential for mitigating greenhouse gas emissions and advancing renewable energy initiatives. However, achieving effective storage necessitates a thorough comprehension of the dynamic interplay between interfacial tension and wettability alteration under varying conditions. This comprehensive review investigates the multifaceted influence of several critical parameters on the alterations of IFT and wettability during the injection and storage of CO2 and hydrogen. Through a meticulous analysis of pressure, temperature, treatment duration, pH levels, the presence of nanoparticles, organic acids, anionic surfactants, and rock characteristics, this review elucidates the intricate mechanisms governing the changes in IFT and wettability within reservoir environments. By synthesizing recent experimental and theoretical advancements, this review aims to provide a holistic understanding of the processes underlying IFT and wettability alteration, thereby facilitating the optimization of storage efficiency and the long-term viability of depleted reservoirs as carbon capture and storage or hydrogen storage solutions. The insights gleaned from this analysis offer invaluable guidance for researchers, engineers, and policymakers engaged in harnessing the potential of depleted reservoirs for sustainable energy solutions and environmental conservation. This synthesis of knowledge serves as a foundational resource for future research endeavors aimed at enhancing the efficacy and reliability of CO2 and hydrogen storage in depleted reservoirs.

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In this work, a beneficial approach for efficient depolymerization of lignin and controllable product distribution is provided. Lignin, an abundant aromatic biopolymer, has the potential to produce various biofuels and chemical adsorption agents and is expected to benefit the future circular economy. Microwave-ultrasonic (MW/US) assisted efficient depolymerization of lignin affords some aromatic materials used in manufacturing the starting material to be investigated. Some nano organometallic surfactants (NOMS) based on Ni2+, Cu2+, Co2+, Fe3+, and Mn2+ besides 2-hydroxynaphth-sulphanilamide are synthesized to enhance oil recovery (EOR). In this work, the assessment of the NOMS's efficiency was improving the heavy oil recovery via the study of the dynamic interfacial tension (IFT), contact angle, and chemical flooding scenarios. The NOMS-Ni2+ exhibited the maximum reduction of viscosity and yield values. Dropping the viscosity to 819.9, 659.89, and 499.9 Pa s from blank crude oil viscosity of 9978.8, 8005.6, and 5008.6 Pa s respectively at temperatures of 40, 60, and 80 °C was investigated. The reduction of τB values was obtained also by OMS-Ni2+. The minimum IFT was recorded against the Ni2+ derivatives (0.1 × 10-1 mN m-1). The complete wettability alteration was achieved with the NOMS-Ni2+ surfactant (ɵ ≅ 6.01 ) . The flooding test has been steered in 3 sets using the sand-packed model as a porous media at surfactant concentrations (1, 1.5, 2 and 2.5%) at 50 °C and 499 psi as injection pressure. The best value (ORs) formed for NOMS-Ni2+ were 62, 81, 85.2, and 89% respectively as compared with other NOMS-M2+ at the same concentrations. The mechanism of alternating wettability was described in the text. The rheology of the used heavy crude oil was investigated under temperatures of 40, 60, and 80 °C.

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Enhanced oil recovery (EOR) processes are technologies used in the oil and gas industry to maximize the extraction of residual oil from reservoirs after primary and secondary recovery methods have been carried out. The injection into the reservoir of surface-active substances capable of reducing the surface tension between oil and the rock surface should favor its extraction with significant economic repercussions. However, the most commonly used surfactants in EOR are derived from petroleum, and their use can have negative environmental impacts, such as toxicity and persistence in the environment. Biosurfactants on the other hand, are derived from renewable resources and are biodegradable, making them potentially more sustainable and environmentally friendly. The present review intends to offer an updated overview of the most significant results available in scientific literature on the potential application of biosurfactants in the context of EOR processes. Aspects such as production strategies, techniques for characterizing the mechanisms of action and the pros and cons of the application of biosurfactants as a principal method for EOR will be illustrated and discussed in detail. Optimized concepts such as the HLD in biosurfactant choice and design for EOR are also discussed. The scientific findings that are illustrated and reviewed in this paper show why general emphasis needs to be placed on the development and adoption of biosurfactants in EOR as a substantial contribution to a more sustainable and environmentally friendly oil and gas industry.

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Despite the positive aspects of low salinity water (LSW), this technique is relatively expensive and unavailable in some countries. Furthermore, potential problems associated with LSW such as scale precipitation in carbonate reservoirs and fine migration in sandstone reservoirs raise concerns. Chelating agents have the ability to chelate metal ions from solution, effectively reducing the salinity of seawater (SW) and mimicking the behavior of LSW. However, they mitigate the challenges associated with LSW injection. This study focuses on how the Diethylenetriaminepentaacetic acid (DTPA) chelating agent performs in modifying rock surface charge. The impact of concentration, brine salinity, potential determining ions (PDIs), oil presence, Fe3+ ions, and solution pH on the effectiveness of DTPA in altering rock surface charge was evaluated. Furthermore, wettability alteration and sand pack flooding tests were conducted to study the effect of DTPA on rock wettability and oil recovery. Results of wettability alteration, zeta potential, sand pack flooding experiments and ion concentration analysis are reported in this paper. The results showed that reducing salinity, increasing DTPA concentration, and raising solution pH changed rock wettability from oil-wetness towards water-wetness. The presence or absence of PDIs in the solution did not affect the performance of DTPA. However, by tripling the concentration of these ions in the solution, the performance of DTPA in changing rock surface charge was impaired. Based on the wettability alteration and zeta potential experiments, 5 wt% DTPA was determined as the optimum concentration. Subsequent flooding experiments revealed that injecting 5 wt% DTPA chelating agents into the sandstone sand pack after SW injection increased oil recovery from 48 % to 68.3 %. The analysis of ion concentrations also revealed a significant increase in the amount of calcium ions during the DTPA flooding, indicating the chelation of metal ions from both rock and solution and improving the wettability conditions.

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HYPOTHESIS: In a porous medium saturated with oil (containing oleic surfactant) and saline water, salinity reduction alters the thermodynamic equilibrium and induces spatial redistribution of surfactants, changing the local fluid configuration. During fluid-fluid displacement, this local change reshapes global fluid flows, and thus results in improved oil displacement. EXPERIMENTS: We performed microfluidic experiments in a centimeter-long pore-network model with a fracture and a dead-end model to observe both the macroscale flows and microscopic fluid configuration evolution. Water with different salinities and model oils with different surfactant concentrations are used. FINDINGS: When oil contacts low salinity water, we observe (1) the solid surface becomes more water-wet, and (2) water-in-oil emulsion spontaneously emerges near the oil-water interface. At the macroscale, the fluid distribution remains unchanged in short term but dramatically changes after tens of hours, which appears as improved oil recovery. Two modes are identified during fluid redistribution: gradual imbibition and sudden collapse. The displacement efficiency is a non-monotonic function of surfactant concentration. This is attributed to the interplay between two opposing effects by adding surfactant: (1) enhancing initial hydrophobicity which negatively affects the displacement, and (2) allowing stronger oil swelling which is beneficial for displacement.

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In the petroleum industry, the remaining oil is often extracted using conventional chemical enhanced oil recovery (EOR) techniques, such as polymer flooding. Nanoparticles have also greatly aided EOR, with benefits like wettability alteration and improvements in fluid properties that lead to better oil mobility. However, silica nanoparticles combined with polymers like hydrolyzed polyacrylamide (HPAM) improve polymer flooding performance with better mobility control. The oil displacement and the interaction between the rock and polymer solution are both influenced by this hybrid approach. In this study, we investigated the effectiveness of the injection of nanofluid-polymer as an EOR approach. It has been observed that nanoparticles can change rock wettability, increase polymer viscosity, and decrease polymer retention in carbonate rock. The optimum concentrations for hydrolyzed polyacrylamide (2000 ppm) and 0.1 wt% (1000 ppm) silica nanoparticles were determined through rheology experiments and contact angle measurements. The results of the contact angle measurements revealed that 0.1 wt% silica nanofluid alters the contact angle by 45.6°. The nano-silica/polymer solution resulted in a higher viscosity than the pure polymer solution as measured by rheology experiments. A series of flooding experiments were conducted on oil-wet carbonate core samples in tertiary recovery mode. The maximum incremental oil recovery of 26.88% was obtained by injecting silica nanofluid followed by a nanofluid-assisted polymer solution as an EOR technique. The application of this research will provide new opportunities for hybrid EOR techniques in maximizing oil production from depleted high-temperature and high-salinity carbonate reservoirs.

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Chemical enhanced oil recovery (EOR) through waterflooding is the most commonly used method to improve crude oil displacement and extraction however; the impact of environmental side effects may remain ambiguous. Regarding, flooding tagged water with tracers provides a better understanding of the fate of injected water and the reservoir conditions more than oil recovery. This study's main focus is the proposed carbon dots (CDs) to develop fluorescent-tagged with dual functions as a sensing and an enhancing agent for EOR operations. Different physicochemical and optical properties were obtained for CDs by tuning the surface chemistry of phenylenediamine (PD) isomers and tartaric acid (TA) via the solvothermal method which leads to green, and yellow fluorescent emissions. Size distribution and colloidal and thermal stability of the prepared nanofluids carrying CDs were controlled by atomic force microscope (AFM), transmission electron microscopy (TEM), dynamic light scattering (DLS), zeta potential, and thermogravimetric analysis (TGA). Long-time emission stability in high temperature and salinity such as conditions found in the oil reservoirs was precisely detected by fluorescence spectroscopy and a portable UV cabinet as the on-site detection method to confirm the sensing ability of CDs. While, rheological parameters of nanofluids such as viscosity, wettability alteration, and fluid/crude oil interfacial tension were evaluated to support the potential of CDs as an enhancing agent to sweep crude oil on the carbonate rock reservoirs. The oil displacement mechanism was monitored on the micromodel pattern by recording 27.8 % and 20.5 % displacement factors for the prepared nanofluids carrying 200 ppm CDs.

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Surface complexation models (SCM), based mainly on the diffuse double layer (DDL) theory, have been used to predict zeta potential at the crude oil-brine-rock (COBR) interface with limited success. However, DDL is inherently limited in accurately predicting zeta potential by the assumptions that all the brine ions interact with the rock surface at the same plane and by the double layer collapse at higher brine ionic strength (>1M). In this work, a TLM-based SCM captured zeta potential trends at the calcite-brine interface with ionic strength up to 3 M. An extended DDL and TLM-based SCMs were used to predict the electrokinetic properties of a composite carbonate rock showing a different mineralogical composition. The extended TLM-based SCM captured the zeta potential prediction trends and magnitude, highlighting the contribution of the inorganic minerals and organic impurities on the composite carbonate surface. In contrast, the extended DDL-based SCM captured the zeta potential trends but failed to capture the magnitude of the measured zeta potential. Interestingly, the TLM-based SCM predicted a positive SP for the rock-brine interface, which could explain the oil-wet nature of composite carbonate rocks due to electrostatic adsorption of negatively charged carboxylic acids. Conversely, the DDL-based SCM predicted a negative SP, leading to an inaccurate interpretation of the electrokinetic properties at the rock-brine interface. Thus, the use of extended TLM-based SCM was required to accurately predict the zeta potential and account for the adsorption of carboxylic acids on the reservoir composite carbonate surface.

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Combinatory flooding techniques evolved over the years to mitigate various limitations associated with unitary flooding techniques and to enhance their performance as well. This study investigates the potential of a combination of 1-hexadecyl-3-methyl imidazolium bromide (C16mimBr) and monoethanolamine (ETA) as an alkali-surfactant (AS) formulation for enhanced oil recovery. The study is conducted comparative to a conventional combination of cetyltrimethylammonium bromide (CTAB) and sodium metaborate (NaBO2). The study confirmed that C16mimBr and CTAB have similar aggregation behaviors and surface activities. The ETA-C16mimBr system proved to be compatible with brine containing an appreciable concentration of divalent cations. Studies on interfacial properties showed that the ETA-C16mimBr system exhibited an improved IFT reduction capability better than the NaBO2-CTAB system, attaining an ultra-low IFT of 7.6 × 10-3 mN/m. The IFT reduction performance of the ETA-C16mimBr system was improved in the presence of salt, attaining an ultra-low IFT of 2.3 × 10-3 mN/m. The system also maintained an ultra-low IFT even in high salinity conditions of 15 wt% NaCl concentration. Synergism was evident for the ETA-C16mimBr system also in altering the carbonate rock surface, while the wetting power of CTAB was not improved by the addition of NaBO2. Both the ETA-C16mimBr and NaBO2-CTAB systems proved to form stable emulsions even at elevated temperatures. This study, therefore, reveals that a combination of surface-active ionic liquid and organic alkali has excellent potential in enhancing the oil recovery in carbonate reservoirs at high salinity, high-temperature conditions in carbonate formations.

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An understanding of clay mineral surface chemistry is becoming critical as deeper levels of control of reservoir rock wettability via fluid-solid interactions are sought. Reservoir rock is composed of many minerals that contact the crude oil and control the wetting state of the rock. Clay minerals are one of the minerals present in reservoir rock, with a high surface area and cation exchange capacity. This is a first-of-its-kind study that presents zeta potential measurements and insights into the surface charge development process of clay minerals (chlorite, illite, kaolinite, and montmorillonite) in a native reservoir environment. Presented in this study as well is the effect of fluid salinity, composition, and oilfield operations on clay mineral surface charge development. Experimental results show that the surface charge of clay minerals is controlled by electrostatic and electrophilic interactions as well as the electrical double layer. Results from this study showed that clay minerals are negatively charged in formation brines as well as in deionized water, except in the case of chlorite, which is positively charged in formation water. In addition, a negative surface charge results from oilfield operations, except for operations at a high alkaline pH range of 10-13. Furthermore, a reduction in the concentrations of Na, Mg, Ca, and bicarbonate ions does not reverse the surface charge of the clay minerals; however, an increase in sulfate ion concentration does. Established in this study as well, is a good correlation between the zeta potential value of the clay minerals and contact angle, as an increase in fluid salinity results in a reduction of the negative charge magnitude and an increase in contact angle from 63 to 102 degree in the case of chlorite. Lastly, findings from this study provide vital information that would enhance the understanding of the role of clay minerals in the improvement of oil recovery.

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We have studied wettability alterations through imbibition/flooding and their synergy with interfacial tension (IFT) for alkalis, nanoparticles and polymers. Thus, the total acid number (TAN) of oil may determine the wetting-state of the reservoir and influence recovery and IFT. Data obtained demonstrate how the oil TAN number (low and high), chemical agent and reservoir mineralogy influence fluid-fluid and rock-fluid interactions. We used a laboratory evaluation workflow that combines complementary assessments such as spontaneous imbibition tests, IFT, contact angle measurements and selected core floods. The workflow evaluates wettability alteration, IFT changes and recovery when injecting alkalis, nanoparticles and polymers, or a combination of them. Dynamics and mechanisms of imbibition were tracked by analyzing the recovery change with the inverse bond number. Three sandstone types (outcrops) were used, which mainly differed in clay content and permeability. Oils with low and high TANs were used, the latter from the potential field pilot 16 TH reservoir in the Matzen field (Austria). We have investigated and identified some of the conditions leading to increases in recovery rates as well as ultimate recovery by the imbibition of alkali, nanoparticle and polymer aqueous phases. This study presents novel data on the synergy of IFT, contact angle Amott imbibition, and core floods for the chemical processes studied.

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A consideration of the negative environmental aspects of fossil fuels has made natural gas the best choice to meet the human demand for energy. The condensate gas reservoir is one source of gases that tolerates skin problems (liquid blockage). Conventional methods for inhibiting or removing liquid blockages are momentary treatments, non-eco-friendly, and expensive. Therefore, new methods have been introduced, such as wettability alteration toward liquid repellency, renewable energies, thermochemical reactions and waves for heating reservoirs, and CO2 injection. This paper reviews the methods for altering the wettability of porous media by fluorochemicals, fluorinated nanoparticles (NPs), and free fluorocarbon materials from natural substances. NPs, particularly silicon-based types, as a green, clean, and emerging technology that are more compatible with the environment, were investigated for their ability to alter the wettability and upgrade conventional materials, such as polymers and surfactants. The feasibility of using renewable energies, thermochemical reactions, and waves for heating the gas condensate reservoir to overcome the skin problem and return the reservoir to the reasonable and economical gas production is reviewed. Finally, CO2 injection is introduced as a multi-purpose green method to enhance gas condensate recovery and allow CO2 sequestration.

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HYPOTHESIS: Surfactant flooding is the leading approach for reversing the wettability of oil-wet carbonate reservoirs, which is critical for the recovery of the remaining oil. Combination of molecular dynamics (MD) simulations with experiments on simplified model systems can uncover the molecular mechanisms of wettability reversal and identify key molecular properties for systematic design of new, effective chemical formulations for the enhanced oil recovery. EXPERIMENTS/SIMULATIONS: Wettability reversal by a series of surfactant solutions was studied experimentally using contact angle measurements on aged calcite chips, and a novel MD simulation methodology with scaled-charges that provides superior description of the ionic interactions in aqueous solutions. FINDINGS: The MD simulation results were in excellent agreement with the experiments. Cationic surfactants were the most effective in reversing the calcite wettability, resulting in complete detachment of the oil from the surface. Some nonionic surfactants also altered the wettability, but to a lesser degree, while the amphoteric and anionic surfactants had no effect. From the tested cationic surfactants, the double-tailed one was the least effective, but the experiments were inconclusive due to its poor solubility. Contributions of specific interactions to the wettability reversal process and implications for the design and optimization of surfactants for the enhanced oil recovery are discussed.

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Low Salinity Water Injection (LSWI) has been a well-researched EOR method, with several experimental and theoretical scientific papers reported in the literature over the past few decades. Despite this, there is still an ongoing debate on dominant mechanisms behind this complex EOR process, and some issues remain elusive. Part of the complexity arises from the scale of investigation, which spans from sub-pore scale (atomic and electronic scale) to pore scale, core scale, and reservoir scale. Molecular Dynamics (MD) simulation has been used as a research tool in the past decade to investigate the nano-scale interactions among reservoir rock (e.g., calcite, silica), crude oil, and brine systems in presence of some impurities (e.g., clay minerals) and additives (e.g., nanoparticles). In this paper, fundamental concepts of MD simulation and common analyses driven by MD are briefly reviewed. Then, an overview of molecular models of the most common minerals encountered in petroleum reservoirs: quartz, calcite, and clay, with their most common types of potential function, is provided. Next, a critical review and in depth analysis of application of MD simulations in LSWI process in both sandstone and carbonate reservoirs in terms of sub-pore scale mechanisms, namely electrical double layer (EDL) expansion, multi-ion exchange (MIE), and cation hydration, is presented to scrutinize role of salinity, ionic composition, and rock surface chemistry from an atomic level. Some inconsistencies observed in the literature are also highlighted and the reasons behind them are explained. Finally, a future research guide is provided after critically discussing the challenges and potential of the MD in LSWI to shed more light on governing mechanisms behind LSWI by enhancing the reliability of MD outcomes in future researches. Such insights can be used for design of new MD researches with complementary experimental studies at core scale to capture the main mechanisms behind LSWI.

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An aqueous suspension of silica nanoparticles or nanofluid can alter the wettability of surfaces, specifically by making them hydrophilic and oil-repellent under water. Wettability alteration by nanofluids has important technological applications, including for enhanced oil recovery and heat transfer processes. A common way to characterize the wettability alteration is by measuring the contact angles of an oil droplet with and without nanoparticles. While easy to perform, contact angle measurements do not fully capture the wettability changes to the surface. Here, we employed several complementary techniques, such as cryo-scanning electron microscopy, confocal fluorescence and reflection interference contrast microscopy, and droplet probe atomic force microscopy (AFM), to visualize and quantify the wettability alterations by fumed silica nanoparticles. We found that nanoparticles adsorbed onto glass surfaces to form a porous layer with hierarchical micro- and nanostructures. The porous layer can trap a thin water film, which reduces contact between the oil droplet and the solid substrate. As a result, even a small addition of nanoparticles (0.1 wt %) lowers the adhesion force for a 20 µm sized oil droplet by more than 400 times from 210 ± 10 to 0.5 ± 0.3 nN as measured by using droplet probe AFM. Finally, we show that silica nanofluids can improve oil recovery rates by 8% in a micromodel with glass channels that resemble a physical rock network.

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The use of engineered water (EW) nanofluid flooding in carbonates is a new enhanced oil recovery (EOR) hybrid technique that has yet to be extensively investigated. In this research, we investigated the combined effects of EW and nanofluid flooding on oil-brine-rock interactions and recovery from carbonate reservoirs at different temperatures. EW was used as dispersant for SiO2 nanoparticles (NPs), and a series of characterisation experiments were performed to determine the optimum formulations of EW and NP for injection into the porous media. The EW reduced the contact angle and changed the rock wettability from the oil-wet condition to an intermediate state at ambient temperature. However, in the presence of NPs, the contact angle was reduced further, to very low values. When the effects of temperature were considered, the wettability changed more rapidly from a hydrophobic state to a hydrophilic one. Oil displacement was studied by injection of the optimised EW, followed by an EW-nanofluid mixture. An additional recovery of 20% of the original oil in place was achieved. The temperature effects mean that these mechanisms are catalytic, and the process involves the initiation and activation of multiple mechanisms that are not activated at lower temperatures and in each standalone technique.

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Nanofluids have shown their potential in the oil recovery process through surface modification. Due to their surface characteristics, they can apply to improve the oil production from reservoirs by enabling different enhanced recovery mechanisms. The preparation and development of the Fe3O4@SiO2 nanoparticles for the oil recovery process is an innovative and novel approach that influences the oil generation from reservoirs. The performance of the Fe3O4@SiO2 and the other nanofluids (seawater, Fe3O4, and SiO2) in the enhanced oil recovery process is assessed and compared with other flooding scenarios. The Fe3O4@SiO2 NPs achieved the highest oil production rate of 90.2% while Fe3O4 and SiO2 NPs achieved 70.8% and 55.3%, respectively. In contrast, the value achieved for the seawater injection was 76.5%. For the oil recovery process, the Fe3O4 was applied for the inhibition (i.e., decrease) of oil sedimentation, and the SiO2 NPs were applied for wettability alteration and IFT reduction. The experimental results showed that the produced Fe3O4@SiO2 NPs improved the oil recovery rates (90.2%) as well as the synergetic impact of the developed NPs by initiating several mechanisms corresponding to the use of the separate NPs in the micromodel. Moreover, the results exhibited that the reservoir conditions are a crucial function for increasing the oil recovery rates, improving the emulsion stability, and acts as a substantial step for the oil recovery method that applies this particular technique.

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The wettability of carbonate rocks is often oil-wet or mixed wet. A large fraction of oil is still remained in carbonate reservoirs, it is therefore of particular significance to implement effective methods to improve oil recovery from carbonate reservoirs. Altering wettability from oil-wet to more favorable water-wet has been proven successful to achieve this goal. Surfactants are widely investigated and served as wettability modifiers in this process. Yet a comprehensive review of altering wettability of carbonate reservoirs with surfactants is ignored in literature. This study begins with illustration of wettability evolution process in carbonate reservoirs. Techniques to evaluate wettability alteration extent or to reveal behind mechanisms are also presented. Several surfactant systems are analyzed in terms of their wettability alteration mechanisms, influential factors of performance, applicable conditions, and limitations. Mixture of different types of surfactants could obtain synergic effects, where applicable conditions are extended, and final performance is improved. Gemini surfactants have many desirable properties, which warrants further investigation for understanding their wettability alteration mechanisms and performance. At the end, this review discusses strategies related with surfactant cost, surfactant adsorption, and challenges at high temperature, high salinity reservoirs conditions. Also, some unclear issues are discussed.

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Laboratory experiments have shown higher oil recovery with nanoparticle (NPs) flooding. Accordingly, many studies have investigated the nanoparticle-aided sweep efficiency of the injection fluid. The change in wettability and the reduction of the interfacial tension (IFT) are the two most proposed enhanced oil recovery (EOR) mechanisms of nanoparticles. Nevertheless, gaps still exist in terms of understanding the interactions induced by NPs that pave way for the mobilization of oil. This work investigated four types of polymer-coated silica NPs for oil recovery under harsh reservoir conditions of high temperature (60 ∘C) and salinity (38,380 ppm). Flooding experiments were conducted on neutral-wet core plugs in tertiary recovery mode. Nanoparticles were diluted to 0.1 wt.% concentration with seawater. The nano-aided sweep efficiency was studied via IFT and imbibition tests, and by examining the displacement pressure behavior. Flooding tests indicated incremental oil recovery between 1.51 and 6.13% of the original oil in place (OOIP). The oil sweep efficiency was affected by the reduction in core's permeability induced by the aggregation/agglomeration of NPs in the pores. Different types of mechanisms, such as reduction in IFT, generation of in-situ emulsion, microscopic flow diversion and alteration of wettability, together, can explain the nano-EOR effect. However, it was found that the change in the rock wettability to more water-wet condition seemed to govern the sweeping efficiency. These experimental results are valuable addition to the data bank on the application of novel NPs injection in porous media and aid to understand the EOR mechanisms associated with the application of polymer-coated silica nanoparticles.