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.

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.

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.

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.

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.

Amphipathic compounds known as biosurfactants are able to reduce surface and interfacial tensions. These substances produced by microbial organisms perform the same functions as chemical surfactants with several enhancements, the most significant of which is biocontrol activity. Lipopeptide is one of the five biosurfactants from natural resources and is identified as the best alternative for chemical surfactants and the major topic of interest for both scientific and industrial communities due to their increasingly growing potential applications in biological and commercial fields. These are the biological compounds with very less toxicity level that increase their importance in the pesticide industry. In this article we summarize the structural diversity of the microbial lipopeptide biosurfactants and focus on their applications as biocontrol agents in plants, covering (1) an intensive study of the structural diversity of lipopeptide biosurfactants originated primarily by the Bacillus, Pseudomonas, Cyanobacteria, and Actinomycetes species is presented, (2) the comparative study of advantages and disadvantages of characterization techniques and physicochemical properties which have a major role in biocontrol activity of microbial lipopeptides, and (3) their wide range biocontrol applications as systemic resistance inducers against different plant diseases, resistance against phytopathogens by alteration of wettability of plant surfaces and antimicrobial activities of important bioactive lipopeptides produced from Bacillus strains.

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.

OBJECTIVE: 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.
METHODS: 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.
RESULTS: 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.

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.

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.