Surfactant Solutions Research Articles

Volumetric and viscometric study on the interaction of amino acid (valine) with an aqueous solution of cationic surfactant, Cetyltrimethylammonium Bromide (CTAB), at 298.15, 303.15, 308.15, and 313.15 K

Interactions between the surfactant (CTAB) and amino acid (valine) were investigated using density and viscosity data. These data were utilized to calculate apparent molar volume, fv, and partial molar volume also known as limiting molar volume f0v and these parameters were further used to find out solute-solvent interactions between amino acid and surfactant at 298.15, 303.15, 308.15 and 313.15 K temperatures.

Pressure Changes Across a Membrane Formed by Coacervation of Oppositely Charged Polymer-Surfactant Systems.

We investigate the mass transfer and membrane growth processes during capsule formation by the interaction of the biopolymer xanthan gum with CnTAB surfactants. When a drop of xanthan gum polymer solution is added to the surfactant solution, a membrane is formed by coacervation. It encapsulates the polymer drop in the surfactant solution. The underlying mechanisms and dynamic processes during capsule formation are not yet understood in detail. Therefore, we characterized the polymer-surfactant complex formation during coacervation by measuring the surface tension and surface elasticity at the solution-air interface for different surfactant chain lengths and concentrations. The adsorption behavior of the mixed polymer-surfactant system at the solution-air interface supports the understanding of observed trends during the capsule formation. We further measured the change in capsule pressure over time and simultaneously imaged the membrane growth via confocal microscopy. The cross-linking and shrinkage during the membrane formation by coacervation leads to an increasing tensile stress in the elastic membrane, resulting in a rapid pressure rise. Afterward, the pressure gradually decreases and the capsule shrinks as water diffuses out. This is not only due to the initial capsule overpressure but also due to osmosis caused by the higher ionic strength of the surfactant solution outside the capsule compared to the polymer solution inside the capsule. The influence of polymer concentration and surfactant type and concentration on the pressure changes and the membrane structure are studied in this work, providing detailed insights into the dynamic membrane formation process by coacervation. This knowledge can be used to produce capsules with tailored membrane properties and to develop a suitable encapsulation protocol in technological applications. The obtained insights into the mass transfer of water across the capsule membrane are important for future usage in separation techniques and the food industry and allow us to better predict the capsule time stability.

Diffusiophoretic Transport of Charged Colloids in Ionic Surfactant Gradients Entirely below versus Entirely above the Critical Micelle Concentration.

When placed in an ionic surfactant gradient, charged colloids will undergo diffusiophoresis at a velocity, uDP = MDP∇ ln S, where MDP is the diffusiophoretic mobility and S is the surfactant concentration. The diffusiophoretic mobility depends in part on the charges and diffusivities of the surfactants and their counterions. Since micellization decreases surfactant diffusivity and alters charge distributions in a surfactant solution, MDP of charged colloids in ionic surfactant gradients may differ significantly when surfactant concentrations are above or below the critical micelle concentration (CMC). The role of micelles in driving diffusiophoresis is unclear, and a previously published model that accounts for micellization suggests the possibility of a change in the sign of MDP above the CMC [Warren, P. B.; . Soft Matter 2019, 15, 278-288]. In the current study, microfluidic channels were used to measure the transport of negatively charged polystyrene colloids in sodium dodecyl sulfate (SDS) surfactant gradients established at SDS concentrations that are either fully above or fully below the CMC. Interpretation of diffusiophoresis was aided by measurements of the colloid electrophoretic mobility as a function of SDS concentration. A numerical transport model incorporating the prior diffusiophoretic mobility model for ionic surfactant gradients was implemented to elucidate signatures of positive and negative diffusiophoretic mobilities and compare with experiments. The theoretically predicted sign of the diffusiophoretic mobility below the CMC was determined to be particularly sensitive to uncertainty in colloid and surfactant properties, while above the CMC, the mobility was consistently predicted to be positive in the SDS concentration range considered in the experiments conducted here. In contrast, experiments only showed signatures of a negative diffusiophoretic mobility for these negatively charged colloids with no change of sign. Colloid diffusiophoretic transport measured in micellar solutions was more extensive than that below the CMC with the same ∇ ln S.

Research note: A scald water surfactant combined with an organic acid carcass dip reduces microbial contaminants on broiler carcasses during processing

Organic acids are applied to poultry carcasses during processing to reduce foodborne pathogens and spoilage microorganisms. Scald water surfactant agents employed to improve feather removal may enhance the efficacy of organic acids during processing. This study investigated the effects of concurrent application of a scald water surfactant and organic acid dip on microbial contamination of carcasses processed in a small-scale production model. Broilers were reared in litter floor pens to 47 d of age and slaughtered using standard practices. Carcasses were scalded in either control or surfactant scald water initially and dipped in either a 2% organic acid blend or water after feather removal to complete a 2 × 2 factorial arrangement with n = 15 carcasses per treatment group. The commercially available scald water additive was a slightly alkaline surfactant solution labelled as a feather removal aid. The organic acid dip consisting of lactic and citric acid was maintained at pH of 2.5. Approximately 10 g of neck skin was collected 1-min postdipping and placed in buffered peptone water with an added neutralizing agent, sodium thiosulfate. Serial dilutions were performed to determine general coliform (GC), E. coli (EC), and aerobic plate (APC) counts as CFU per gram of skin sample. A significant 0.61, 0.76, and 1.6 log reduction of GC, EC, and APC, respectively, was attributed to use of the organic acid carcass dip (P ≤ 0.01). There were no significant differences in carcass microbial reduction due to surfactant scald water alone. A 0.69, 0.73 (P ≤ 0.05), and 1.96 log reduction of GC, EC, and APC, respectively, was observed in surfactant-scalded, acid-dipped carcasses compared to water-scalded, water-dipped control groups. These data demonstrated that a surfactant scald water additive and an organic acid carcass dip can have beneficial effects of microbial reduction when employed simultaneously during broiler processing.

Synergisms between Surfactants, Polymers, and Alcohols to Improve the Foamability of Mixed Systems

In order to produce detergents with improved performance and good market acceptability, it is crucial to develop formulations with improved foamability and cleaning performance. The use of a delicate balance of surfactants and additives is an appealing strategy to obtain good results and enables a reduction in the amount of chemicals used in formulations. Mixtures of hydrophobically modified linear polymers and surfactants, as well as balanced mixtures with co-surfactants and/or hydrotropes, are the most effective parameters to control foamability and foam stability. In the present study, the effect of the addition of hydrophobically modified linear polymers, nonionic co-surfactants and hydrotropes, and their mixtures to anionic and zwitterionic surfactant aqueous solutions was evaluated. It was found that the presence of the hydrophobically modified polymer (HM-P) prevented the bubbles from bursting, resulting in better stability of the foam formed using zwitterionic surfactant solutions. Also, the surfactant packing was inferred to be relevant to obtaining foamability. Mixtures of surfactants, in the presence of a co-surfactant or hydrotrope led, tendentially, to an increase in the critical packing parameter (CPP), resulting in higher foam volumes and lower surface tension for most of the studied systems. Additionally, it was observed that the good cleaning efficiency of the developed surfactant formulations obtained a higher level of fat solubilization compared to a widely used brand of commercial dishwashing detergent.

An ESIPT-Based Fluorescent Probe for Wash-Free Cell Membrane Imaging.

The cell membrane tracking is important for studying the membrane function and diagnosing membrane-related diseases, so the development of fluorescent molecule specifically lighting up cell membrane is highly desirable. In this work, we designed and readily prepared a fluorescent dye (BOHI) that can target cell membrane. The pH-dependent emission spectra reveal that BOHI shows fluorescence based on the excited-state intramolecular proton transfer (ESIPT) under acidic and neutral conditions, while the blue-shifted emission from the phenolate anion of BOHI was observed when pH ≥ 9. Among various solvents, the weakest fluorescence emission was observed in H2O, which is favorable to wash-free imaging. The fluorescence intensity of BOHI is greatly affected by surfactants. The anionic surfactant can induce intense green fluorescence, while very weak fluorescence was observed in the solution of cationic surfactant. Hela cells images show that BOHI can specifically targets and lights up cell membrane.

New long tail gemini surfactant in aqueous solution: Self-assembly, rheological properties and responsiveness to hydrocarbon

Gemini surfactants are promising to replace conventional monomeric surfactants in various applications. In this paper, a new gemini surfactant with long unsaturated oleyl tails and bis(hydroxyethyl) ammonium head groups linked by butyl spacer was synthesized. Its critical micelle concentration in salt-free water (12 µM) is much lower than for its monomeric analog (220 µM). Without any additives this surfactant can form viscoelastic solutions with the viscosity of up to 1 kPa·s and elastic modulus of 15 Pa at the conditions, when the viscosity of the single-chained monomeric analog is close to that of pure water. These are one of the highest values reported so far for C18-tailed gemini surfactants without additives. The structure of the gemini surfactant solutions was studied by cryo-TEM and SAXS. Cryo-TEM revealed the presence of closed-looped micelles coexisting with linear wormlike micelles as well as the regular spacing between the micelles arising from strong electrostatic repulsion between them. The SAXS curves were well-fitted by a form-factor of core–shell cylinder, which yielded the radius of the core and the thickness of the shell equal to 1.4 nm each. Addition of n-decane induced the drop of viscosity by 6 orders of magnitude accompanied by the transformation of wormlike micelles into microemulsion droplets with 4.4 nm radius. Such gemini surfactants providing high viscoelasticity to aqueous solution that is responsive to added hydrocarbon are promising for the application in oil recovery as thickeners of fracturing fluids that can be cleaned up without any breakers at the backflow of oil.

Laboratory study on the performance of AOS surfactant in increasing oil recovery

The decline in oil recovery in the oil and gas field is a problem that must be faced along with increasing energy needs. Efforts are made to increase oil recovery reserves with advanced methods, namely Enhanced Oil Recovery. In this study, an AOS (alpha olefin sulfonate) surfactant solution was used. Tests were conducted with varying concentrations at a salinity of 7,000 ppm. Phase behavior tests were also conducted for 7 days at 80 °C. The oil recovery value of the surfactant solution was also investigated. The testing stages carried out were density, interfacial tension, and core flooding tests. After making the surfactant solution sample, a density test was conducted at 30 and 80 °C. Finally, the core flooding test. The IFT results of the surfactant solution reached the critical micelle concentration (CMC) point so that it could reduce the interfacial tension well between oil and formation water in the reservoir with an interfacial tension value of 0.8212087 dyne/cm. Core flooding results are based on surfactants that reach the CMC point. There is a surfactant with a concentration of 1% Salinity 7,000 ppm at the CMC point with a recovery factor of 7.2727%.

Integrating low salinity water, surfactant solution, and functionalized magnetite nanoparticles with natural acidic groups for enhanced oil recovery: Interfacial tension study

In recent years, nanoparticles (NPs) have become a popular choice for improving oil recovery through enhanced oil recovery (EOR) methods. NPs can enhance oil recovery by reducing interfacial tension (IFT), altering wettability, and decreasing the mobility ratio. In this study, magnetic NPs with acidic groups (tartaric acid and malic acid), which are natural acids found in fruits such as grapes and apples, were synthesized and functionalized to reduce the IFT between oil and water. Various characterizations tests, including zeta potential (ZP), Fourier transform infrared spectroscopy (FTIR), X-ray diffraction analysis (XRD), dynamic light scattering (DLS), field emission scanning electron microscopy (FE-SEM), and energy dispersive X-ray analysis (EDAX), were used to determine the properties of NPs. Afterwards, the IFT behaviour of crude oil and aqueous solutions, containing surfactant sodium dodecyl sulfate (SDS), two types of salts namely sodium chloride (NaCl) and sodium sulfate (Na2SO4), and functionalized magnetite NPs with tartaric acid and malic acid were investigated. Two crude oils were used in this study: light (A) and heavy (B). The results showed that increasing salt concentration decreases the IFT for crude oils down to an optimum point (20000 ppm for both salts), after which the IFT increases with increasing salt concentration. The presence of functionalized Fe3O4@Tartaric acid NPs (300 ppm) in the aqueous solutions containing salts at their optimum concentration (20000 ppm) and SDS (300 ppm) can decrease the IFT more significantly than that of Fe3O4 and Fe3O4@Malic acid for both crude oils. This is due to higher stability and higher ZP of functionalized Fe3O4@Tartaric acid NPs compared to Fe3O4@Malic. The IFT for oil A decreases from 20.8 mN/m to 2.87 mN/m for light crude oil and from 32.96 mN/m to 1.91 mN/m for heavy crude oil. The IFT for heavy crude oil was more reduced than that of light crude oil, which was due to the presence of asphaltene, resin, and other surface-active agents in heavy crude oil, which can act as a natural surfactant in oil and help reducing the IFT.

How triacylglycerol thermal history impacts film removal by surfactant solution

Hypothesis: The physical and mechanical properties of triacylglycerols (TAGs), or ‘fats’, depend on their composition and thermal history which, in turn, impact crystal structure and morphology. We examine whether thermal history can be mechanistically related to film removal by a surfactant solution.Experiments: Model TAG mixtures, comprising triolein:tripalmitin:tristearin 0.5:0.3:0.2, were subjected to a range of cooling profiles from the melt (0.5-80°C/min, Newtonian and annealed), and the resulting solid films characterised by microscopy, X-ray diffraction, infrared spectroscopy, and contact angle measurements. Film removal from a model glass substrate by an aqueous surfactant solution of sodium dodecylsulphate and dodecyldimethylamine oxide at room temperature fixed at 25°C was examined under quiescent flow conditions.Findings: Quantitative relations are established between TAG cooling profile, crystal structure and morphology, surface energy γSFE, and removal (or ‘cleaning’). In general, films cooled slowly from the melt yield heterogeneous morphologies with predominantly β1′ phase, higher polar γSFE, and faster removal timescales. By contrast, rapid cooling results in homogeneous films, rich in β2′ phase, low polar γSFE, and long removal times. Our results elucidate the non-trivial impact of TAG thermal history, connecting the multiscale semi-crystalline structure to surface energy, and eventually to film delamination by micellar solutions.

Promote or inhibit turbulence drag reduction behavior of surfactant solutions with different micelle structures by certain nanoparticle addition

The micelle structure of surfactant is easy to be destroyed in the flow process resulting in a decrease in its drag reduction (DR) efficiency; therefore, how to strengthen the stability of the micelle structure during the flow process and thus improve the drag reduction efficiency deserves intensive research. In this work, by comparing a variety of nanoparticles, hydrophobic silica nanoparticles were selected as the best additive to enhance the turbulence drag reduction efficiency of surfactant solution with spherical micelle structure. The experimental results also demonstrated that the hydrophobic silica nanoparticles had a reinforcing effect on anionic, cationic, nonionic, and zwitterionic surfactant solutions with the same concentration (dominated by spherical micelles), and the optimal nanoparticle addition concentration and maximum drag reduction rate were obtained. Meanwhile, the effect of silica nanoparticles on the turbulence drag reduction efficiency of surfactant solutions with different micelle structures was evaluated by inducing the surfactant micelle structure change. It was shown that the hydrophobic silica nanoparticles had a strengthening effect on the turbulence drag reduction performance of surfactant solutions with spherical micelle structure, while they had an inhibiting effect on the turbulence drag reduction performance of surfactant solutions with worm-like micelle structure. The change in solution viscoelasticity indicated that the decrease in viscoelasticity was the main reason for the decrease in drag reduction efficiency of surfactant solution with worm-like micelle structure when silica nanoparticles were added. A mechanism for the interaction of hydrophilic/hydrophobic silica nanoparticles with spherical micelles and wormlike micelle structures was finally discussed and proposed.

Investigating the foaming behavior of a soybean derived surfactant for gas well deliquification in a sparger setup

Surfactant injection is one of the common gas-well deliquification techniques to enhance gas productivity. However, most traditional chemical-based surfactants are often nonbiodegradable, toxic, and lead to environmental and potential health risks. There is a need to investigate surfactants of natural origins, soybean derived surfactants (SODS) offer promising eco-friendly alternatives. It is crucial to understand the foaming behavior of the biosurfactant and its effectiveness in the deliquification process. Therefore, the main objective of this study is to carry out a comprehensive analysis of the foaming characteristics of SODS and correlate its dynamic surface tension to the foaming properties of other known surfactant solutions using a sparger setup.The results showed that the SODS can generate stable foams and have the potential to mitigate liquid loading problems in gas wells. The bubble formation at the tip of the sparger is highly dependent on the bubble size and foam drainage, so, the surface tension reduction rate is inversely proportional to the bubble radius for all the surfactants under study. Consequently, the total foam weight and foam density of SODS are determined at the top of the production column of the experimental setup, hence the liquid content of the foam () determines the foam formation for the biosurfactant. Also, the foaming qualities in terms of foamability and foam stability increase with maximum for the all the surfactants used. The sparger configuration agrees with the Ross-Miles test for and with the R2 value of 0.91 The study offers a novel strategy for effective gas well deliquification using surfactants with natural origins, furthering sustainable practices in the oil and gas production sector.

Foam fractionation for the separation and enrichment of trace m-phenylenediamine and o-phenylenediamine in solution

In this study, a foam fractionation technique was developed for the separation and enrichment of the trace m-phenylenediamine (MPD) and o-phenylenediamine (OPD) in solution. Firstly, a self-designed foam fractionation device was assembled and built, followed by a comprehensive characterization on gas types, foam fractionation column parameters, and porous sieve plate material used in the apparatus. Subsequently, the most crucial parameters for the separation and enrichment, such as surfactant species, solution pH, electrolyte categories, and gas flow rate, were identified and optimized. The mechanisms of key processes during foam fractionation under the influence of these parameters were thoroughly discussed. Other influencing factors, such as surfactant concentration, foam collection time, and solution volume in the fractionation column, were optimized using response surface methodology (RSM). Under these optimal conditions, maximal enrichment ratios of 138.2 and 85.5 were achieved for MPD and OPD, respectively. Finally, foam fractionation coupled with high-performance liquid chromatography (HPLC) was employed to detect MPD and OPD in the solution. The results demonstrated limits of detection (LOD) of 1.5 × 10−2 μg/L and 1.5 μg/L for MPD and OPD, with relative standard deviation (RSD) values of 4.1 % and 3.9 %. When testing various actual samples, the recoveries were in the range from 92.0 % or greater in all cases. The method exhibited advantages of high sensitivity, precision, and accuracy, attributed to the high enrichment efficiency of foam fractionation. In conclusion, the foam fractionation method established in this study offers simplicity in apparatus, operational convenience, environmental friendliness (minimized use of organic solvents), and high enrichment efficiency. It proves valuable for the quantitative analysis of trace amounts of MPD and OPD in solution, presenting a novel approach for the detection of trace organic compounds in solutions.

Flow pattern and pressure loss of foam flow in horizontal pipes: Role of surfactant type and dynamic surface tension

In this work, the flow patterns and pressure losses of 12 kinds of gas–liquid systems (two different surfactants were selected, and their concentrations were changed in an aqueous solution, which served as the test liquid) in horizontal pipes were studied. To explore the potential mechanisms influencing flow patterns, the equilibrium and dynamic surface tensions of surfactant solutions were surveyed, and the aggregate morphologies of surfactants were observed by using cryo-TEM. Based on the experimental findings, a generalized flow pattern map was proposed. Furthermore, the relationship between the pressure loss and the flow pattern of the foam flow was investigated. The results revealed two types of foam flow: full-foaming flow (FFO) and foam flow containing liquid (FCL). Each type of flow had three subflow patterns. The formation of different flow patterns is closely related to the ability of surfactant molecules to adsorb on bubbles and reduce surface tension in a short period, which is affected by aggregates and their structures. The product of the Weber and Bond numbers was determined to be the appropriate combination of non-dimensional numbers for the proposed generalised flow pattern map. Moreover, above a critical Bond number of the gas–liquid system, FFO cannot be formed. Finally, the flow pattern can be effectively separated according to pressure drop data.

A biosensor method based on surfactant-mediated surface droplet evaporation for the detection of Aflatoxin B1

Aflatoxin B1 (AFB1) is a common mycotoxin that is of significant global concern due to its impact on food safety. Herein, we innovatively develop a sensing platform to detect AFB1 based on evaporation of surfactant solutions on the hydrophobic surface, resulting in dried patterns with varied sizes. The surfactant CTAB solution produces a relatively large dried pattern due to the surface wetting. However, the reduction in the dried pattern size is found when the mixture of CTAB and AFB1 aptamer is tested, because the formation of CTAB/aptamer complex. Moreover, the dried pattern size of the mixture of CTAB, aptamer, and AFB1 increases due to the specific binding of AFB1 to its aptamer. Using this innovative strategy, the AFB1 detection can be fulfilled with a detection limit of 0.77 pg/mL. As a simple, convenient, inexpensive, and label-free method, the surfactant-mediated surface droplet evaporation-based biosensor is very promising for various potential applications.

Understanding the Impact of Fuel on Surfactant Microstructure of Firefighting Foam

AbstractAqueous film-forming foam is being phased out due to the environmental impacts of fluorinated surfactants contained in the firefighting foams. To develop an environmentally friendly firefighting foam, it is important to understand the factors controlling the firefighting performance of surfactants. Fuel transport through foam has been considered as a dominant mechanism for foam collapse. Therefore, the impact of fuels (heptane, octane and trimethylbenzene (TMB)) on surfactant microstructure was studied for three different types of surfactants (Capstone, Glucopon, and siloxane) that have applications in firefighting foam. Multiple techniques were used to identify the microstructure and interfacial properties of surfactants with and without exposure to liquid fuel. The ignition time of fuel vapor through foam and solubility of fuel through liquid surfactant solution were measured as well. This work shows fuel solubility has an impact on the surfactant microstructure and interfacial properties. In addition, fuel solubility and vapor pressure affect the ignition time of fuel vapors.

Oil spill dispersant formulation from Palmitoyl-DEA and methyl ester sulfonate

Surfactants are chemical compounds that can interact with solvents to reduce surface tension. Palmitoyl-Diethanolamide surfactant (Palmitoyl-DEA) and methyl ester sulfonate (MES) can be applied in dispersing oil in seawater as Oil Spill Dispersant (OSD). An OSD formulation derived from a mixture of two surfactant solutions, namely Palmitoyl-DEA and MES, was found. Diethanolamide non-ionic surfactant solution and anionic methyl ester sulfonate surfactant solution in various concentrations were mixed according to their respective ratios at 50℃ for 60 minutes. The OSD product obtained was then analyzed for density, surface tension, and emulsion stability. OSD products at a concentration of 4% MES and 2% DEA with a 2:1 ratio obtained the best analytical results. The OSD product has excellent density, surface tension, and emulsion stability (> 80%). Furthermore, testing of OSD products was carried out for oil pollution in seawater. The results of simulation tests using OSD products for handling petroleum pollution in seawater (15 mL/L) show an excellent ability to disperse oil (> 90%). The oil and OSD dispersed in seawater showed a more significant increase in COD and BOD values.

Formation of Alternating Surfactant-Enriched and Surfactant-Depleted Phases in the Taylor Cone of a Nanoelectrospray.

The electrospray ionization of highly conductive solutions containing Triton X-100, a nonionic surfactant, is found to induce alternating periods of surfactant enrichment and depletion when the concentration of the surfactant is near the critical micelle concentration (CMC) and when the flow rate is on the order of 10 nL/min. Analyzing the surfactant-protein mixture shows that the protein is partially denatured during the surfactant enrichment. The measurement of the phospholipid and oligosaccharide mixture prepared in the surfactant solution shows that the ion signal of the lipid is in phase with, and the hydrophilic oligosaccharide is out of phase with the surfactant signal. The results suggest that this novel phenomenon can be exploited for in situ separation of compounds in ESI-MS. Besides the ion signal, the condition of the alternating phase is also reflected in the spray current and Taylor cone's apex angle. The phase separation is likely related to the formation of a micelle in the Taylor cone and can be selectively triggered by tuning the flow rate with emitter voltage for an on-demand application.

Wet SPF: A wet powder suspension for the detection of latent fingermarks on the sticky side of adhesive tape for use in Seychelles

WET UCIO is an inexpensive carbon-based powder suspension, reportedly as effective as commercially available formulations for latent fingermark detection on the sticky side of adhesive tapes. However, the surfactant solution used in WET UCIO is not readily accessible outside Europe, limiting its use in Seychelles or other non-European jurisdictions. In this study, the UCIO formulation was modified based on a ‘frugal forensic’ approach, by replacing the surfactant solution with an in-house sodium dodecyl sulfate solution prepared in 5 % aqueous ethanol. A comparative assessment against Wetwop™ using eight different pressure-sensitive adhesive tapes found that the modified formulation was at least as effective as commercial powder suspension. Modifying this technique under the frugal forensic framework has enhanced its accessibility to other jurisdictions and is recommended for validation in Seychelles.

Analysis of the Influence Mechanism of Nanomaterials on Spontaneous Imbibition of Chang 7 Tight Reservoir Core

This study investigates the impact of nanomaterials on different surfactant solutions. By measuring the parameters (including emulsification property, zeta potential, DLS, CA, IFT, etc.) of imbibition liquid system with nanoparticles and without nanoparticles, combining with imbibition experiments, the law and mechanism of improving the imbibition recovery of nanomaterials were obtained. The findings demonstrate that the nano-silica sol enhances the emulsification and dispersion of crude oil in the surfactant system, resulting in smaller and more uniform particle sizes for emulsified oil droplets. Non-ionic surfactant AEO-7 has the best effect under the synergistic action of nanomaterials. Zeta potential and DLS tests also showed that AEO-7 exhibits smaller particle sizes due to their insignificant electrostatic interaction with nanoparticles. Furthermore, the addition of nanomaterials enhances the hydrophilicity of core and reduces the interfacial tension. Under the synergistic action of nanoparticles, AEO-7 still showed the best enhanced core hydrophilicity (CA 0.61° after imbibition) and the lowest interfacial tension (0.1750 mN·m−1). In the imbibition experiment, the imbibition recovery of the system with nanomaterials is higher than that of the non-nanomaterials. The mixed system of AEO-7 and nano-silica sol ZZ-1 has the highest imbibition recovery (49.27%). Combined with the experiments above, it shows that nanomaterials have a good effect on enhancing the recovery rate of tight core, and the synergistic effect of non-ionic surfactant AEO-7 with nanomaterials is the best. Moreover, nanomaterials reduce adhesion work within the system while improving spontaneous imbibition recovery. These findings provide theoretical guidance for better understanding the mechanism behind nanomaterial-induced imbibition enhancement as well as improving tight oil’s imbibition recovery.