Surface Tension Measurements Research Articles

Thermodynamic characteristics and surface free energy analysis of bifonazole and lecithin with sodium dodecyl sulfate in hydroethanolic solvent systems

The thermodynamic investigations of the well-recognised antifungal drug bifonazole and lecithin with anionic surfactant sodium dodecyl sulphate have been established. The experiments were conducted using five distinct hydro-ethanolic concentrations, namely 0% v/v, 10% v/v, 30% v/v, 70% v/v, and 90% v/v ethanol, throughout a range of five temperatures (ranging 20 ℃, 25 ℃, 30 ℃, 35 ℃ and 40 ℃) with an increment of drug concentration. The study involved the determination of several parameters, including surface tension (σ), density (ρ), conductivity (κ), contact angle (θ) and surface free energy. Conductivity and surface tension data was used for calculating critical micelle concentration (CMC). CMC was utilised to calculate various thermodynamic properties, such as the standard entropy change (ΔS°m), standard Gibbs energy change (ΔG°m) and standard enthalpy change (ΔH°m) of micellization. This study represents a comparative analysis of the critical micelle concentration (CMC) by utilising surface tension and conductivity measurements. Contact angle is used to determine the hydrophobicity and hydrophilicity of the system. These investigations are valuable for examining the magnitude of hydrophobic interactions within the system, which might be used to ascertain an optimal concentration of bifonazole, lecithin and surfactant to prepare ethosomal formulations.

Experimental study on the measurement criteria for measuring surface tension in oil/refrigerant mixtures by maximum bubble pressure method

Refrigeration oil used in refrigeration compressors is usually compatible with refrigerant. The properties of the mixture are changed when refrigeration oil and refrigerant are mixed in the oil sump of the compressor because the refrigerant dissolves in the oil. Surface tension is one of the properties of the oil/refrigerant mixture that changes during the dissolving process. This change in property has an impact on foaming and the production of oil mist in compressors. In addition, surface tension can be utilized as an indicator of refrigerant concentration in oil. Hence, it is essential to determine the surface tension of the oil/refrigerant mixture. This study employed the maximum bubble pressure method (MBPM) to measure the surface tensions of the refrigeration oil and refrigerant mixtures. The oil was polyvinyl ether (PVE), while the refrigerants were difluoromethane (R32) and R410A, which was a blend of R32 and pentafluoroethane (R125). Since the viscosity of refrigeration oil changed dramatically with the dissolution of refrigerant, the measurement criterion of the MBPM applicable to a wide range of viscosities was clarified using silicone oil with various viscosities. Based on the findings of the surface tension of the PVE/R410A and PVE/R32 mixtures, a predictive formula was presented to estimate the mixture’s surface tension as a function of temperature and refrigerant concentration in oil. Relationships between the refrigerant concentration and normalized surface tension were also proposed.

Applicability of cationic surfactants, anionic surfactants, and nonionic surfactants as foaming agents for foamed concrete: surface activity, foamability, and interaction with cement

Selecting the appropriate surfactant as a foaming agent is crucial in the production of foamed concrete. In this study, multiple technological approaches were employed for the investigation of the effect of three different types of surfactants as foaming agents; the approaches included surface tension measurement, zeta potential analysis, spectrophotometry, and nanoindentation. The results showed that the surface activity, solution viscosity, and environmental pH all influenced the generation and stability of foam in foaming agents. The adsorption process of surfactants onto cement particles was complex and could be effectively explained using the double-layer theory. The adsorption of anionic surfactant molecules on cement particles significantly altered the zeta potential, up to −17 mV, with an adsorption efficiency over 10 times greater than that of cationic surfactants and more than 5 times greater than that of nonionic surfactants. Furthermore, after cement hardening, the mechanical properties of the resulting pores were notably improved due to the presence of adsorbed anionic surfactants, and the maximum compressive strength could exceed 10 MPa.

Marangoni flows triggered by cationic-anionic surfactant complexation

HypothesisThe gradients in surfactant distribution at a fluid-fluid interface can induce fluid flow known as the Marangoni flow. Fluid interfaces found in biological and environmental systems are seldom clean, where mixtures of various surfactants are present. The presence of multi-component surfactant mixtures introduces the possibility of interactions among constituents, which may impact Marangoni flows and alter flow dynamics. ExperimentsWe employed flow visualization, surface tension and reaction kinetic measurements, and numerical simulations to quantitatively investigate the Marangoni flows induced by the reacting surfactant mixtures. Different binary surfactant mixtures were utilized for comparative analysis. FindingsThe impact of surfactant interactions on Marangoni flows is confirmed through the observation of diverse complex flow patterns that result from the combination of oppositely charged surfactants in varying composition ratios and concentrations. Unique flow patterns originate from the composition-dependent interfacial phenomena upon mixing surfactants. Our findings provide vital insights that could be used to guide the development of effective oil remediation or the spreading of waterborne pathogens in contaminated regions.

An experimental design approach to modeling water-free foams

In order to create more eco-friendly products, the industry (such as cosmetics) needs to reduce water consumption, not only in the processing stages but also in the composition of the products themselves. However, water-free products remain challenging, especially in terms of formulation. This paper presents an experimental design approach to model the structure-function properties of natural, biodegradable, and water-free oil foams stabilized with a sucrose ester. In particular, the effects of the sucrose ester concentration and foam-whipping time on foams’ bubble size, size distribution, over-run, and firmness were studied. Also, through surface tension measurements, the bubbles’ surface coverage by the sucrose esters was calculated. In addition, oil/sucrose ester mixtures were prepared at varying mixing temperatures (70, 80, 90, 100 °C) and mixing time durations (1, 5, 24, 72 h) and then whipped causing a direct effect on the foams’ physical properties. The resulting water-free foams had high over-runs (up to 74 %) with a stability of more than 5 months at 25 °C.

Thermodynamics of micellization of octyltrimethylammonium bromide in 1,2-propanediol-water mixtures at temperatures from (293.15 to 308.15) K

The micellar properties of octyltrimethylammonium bromide (C8TAB) in both water and aqueous solutions of 1,2-propanediol have been investigated using accurate measurements of density, sound velocity, and surface tension in the temperature range between 293.15 and 308.15 K. The critical micelle concentration, CMC, the ionization degree, β, the standard thermodynamic parameters of micellization: free energy, ΔmicG°, enthalpy, ΔmicH°, entropy, ΔmicS° and the free energy of transfer, ΔtrG°, of the surfactant octyltrimethylammonium bromide in both water and 1,2 propanediol aqueous solution were evaluated from the experimental results.The CMC of the surfactant increases as the concentration of 1,2-propanediol increases, while the temperature does not exert important changes within the range considered.The value of the micellization thermodynamic parameters suggests that adding 1,2-propanediol makes the micellization process less favorable.The thermodynamic functions of transfer were calculated. The values of the free energy of transfer are small and positive and increase as the diol concentration increases confirming that the transfer of the surfactant from the bulk into the micelle is less favorable.

Exploring the Correlation of Dynamic Surface Tension with Antimicrobial Activities of Quaternary Ammonium-Based Disinfectants.

Quaternary ammonium compound (QAC) disinfectants represent one of our first lines of defense against pathogens. Their inhibitory and bactericidal activities are usually tested through minimum inhibitory concentration (MIC) and time-kill assays, but these assays can become cumbersome when screening many compounds. We investigated how the dynamic surface tension (DST) measurements of QACs correlate with these antimicrobial activities by testing a panel of potent and structurally varied QACs against the gram-positive Staphylococcus aureus and the gram-negative Pseudomonas aeruginosa. We found that DST values correlated well with bactericidal activity in real-world disinfection conditions but not with MIC values. Moreover, no correlation between these two antimicrobial activities of QACs (bactericidal and inhibition) was observed. In addition, we observed that the bactericidal activity of our QAC panel against the gram-negative P. aeruginosa was severely affected in the presence of hard water. Interestingly, we found that the counterion of the QAC affects the killing of bacteria in these conditions, a phenomenon not observed in most MIC assessments. Moreover, some of our best-in-class QACs show enhanced bactericidal activity when combined with a commercially available QAC. In conclusion, we determined that an intrinsic physical property of QACs (DST) can be used as a technique to screen for bactericidal activity of QACs in conditions that mimic real-world disinfection conditions.

Thermodynamic characteristics and aggregation behavior of surface active ionic liquids in presence of vitamin B7 (biotin)

Abstract This study investigated the influence of vitamin B7 (biotin) at different concentrations (0.1, 0.3 and 0.5) mM on the micellisation behaviour of three different ionic liquids with different cationic headgroups, namely N-methylmorpholinium bromide [Mor1,12][Br], N-dodecyl-N-methylpyrrolidinium bromide [Pyrr1,12][Br], and 1-dodecyl-3-methylimidazolium bromide [C12mim][Br], at four different temperatures (298.15, 303.15, 308.15, and 313.15) K using electrical conductivity and surface tension measurements. The evaluated CMC values for the studied system were used to obtain information about the colloidal behavior of the ionic liquids in the presence of biotin. The different thermodynamic parameters were studied. Tensiometry was used to determine the interfacial properties. The parameters obtained were used to study the different types of interactions for micelle formation. The main objective of studying these interactions is to further utilize this type of mixture in pharmaceutical industry, medicinal chemistry, and bio industry.

Preparation and characterization of hydrophobically-modified sodium alginate derivatives as carriers for fucoxanthin

Micelles are nano-architectured structures capable of encapsulating hydrophobic substances in aqueous solutions, thereby improving their stability, solubility, and bioavailability to control the release of bioactive compounds. In this study, the sodium alginate backbone was modified via a hydrophobic modification scheme where octyl chains were covalently attached to the alginate chains via esterification reactions. Fourier-transformed infrared spectrometry (FTIR), 1H nuclear magnetic resonance (1H NMR), X-ray diffraction (XRD), and thermal gravimetric analysis (TGA) were used to characterize the structure of the sodium alginate derivatives of varying molar mass (ALG-C8). Fluorescence spectroscopy, surface tension measurements, and dynamic light scattering (DLS) were employed to assess the self-assembly performance of ALG-C8. The three methods produced consistent results, indicating that self-assembly decreased with higher molar mass. The self-assembled ALG-C8 micelles were utilized to encapsulate fucoxanthin. The loading capacity (LC) and encapsulation efficiency (EE) were determined using UV–Vis spectrophotometry. The molar mass of ALG-C8 has a key influence on fucoxanthin loading and release behavior. The ALG-C8 molecules with the lowest molar mass produced micelles with the smallest hydration diameter, resulting in the highest LC and EE. Furthermore, the release of fucoxanthin is significantly influenced by the pH and ionic strength of the medium. ALG-C8 micellar-like aggregates exhibit resistance to low pH and high ionic strength environments, releasing encapsulated material at the target site under alkaline conditions. Therefore, synthesized ALG-C8 is a potential candidate for preparing pH-responsive self-assembled micellar-like aggregates, enabling targeted delivery and gradual release of hydrophobic functional food components.

The inhibition mechanism of esterified starch on flotation separation of fluorite and calcite

Herein, the flotation behavior of fluorite and calcite was examined before and after starch esterification through mineral flotation experiments. Moreover, the adsorption action mechanisms on minerals before and after starch esterification were investigated using methods such as solution surface tension measurement, infrared spectroscopy, and extended Derjaguin–Landau–Verwey–Overbeek theory. The results showed that after starch esterification (esterified starch), there was a greater difference in the mineral recovery rate compared to before starch esterification (ordinary starch), with a better inhibition effect on calcite. The interaction between mineral surfaces and ordinary starch was weaker than the interaction between minerals and esterified starch. In particular, after starch esterification, the surface tension increased, two minerals contact angle decreased, the surface potential became more negative, and the difference in the mineral recovery rate was greater than before starch esterification. After the interaction between minerals and esterified starch, calcite particles displayed good dispersibility, while the cohesion between calcite particles and sodium oleate particles decreased; notably, the effect on fluorite was opposite. Calcite and esterified starch exhibited chemical adsorption, impeding the adsorption of sodium oleate onto calcite and resulting in calcite inhibition. The interaction between fluorite surface and esterified starch involved electrostatic adsorption, with sodium oleate chemically adsorbed onto the fluorite surface. Chemical adsorption proved stronger than electrostatic adsorption, enabling sodium oleate to capture fluorite.

Synergistic effects of an amphiphilic drug(propranolol hydrochloride) with cationic surfactants in an aqueous medium: A physicochemical study

The interactions of amphiphilic drug(propranolol hydrochloride, PPL) with cationic surfactants, such as dodecyltrimethylammoniumbromide(DTAB), tetradecyltrimethylammonium bromide (TTAB), trimethyltetradecylammonium chloride(TTAC) and tetyltrimethylammonium bromide(CTAB), in an aqueous medium were evaluated. The surface tension measurement was used to examine the mixed micellization behavior and surface properties of drug-surfactant mixtures. The nonideal or synergistic behaviors of the mixed systems were explored by using several physical models, such as Clint, Rubingh, Rosen, and Motomura models, based on regular solution theory and pseudophase approximation. In addition, the synergism between PPL and cationic surfactants was also confirmed using ultraviolet–visible spectroscopy. The stoichiometric ratios, binding constants, and free energy changes of the drug–surfactant mixtures were computed using Benesi–Hildebrand (B–H) theory.

Surface tension measurement and molecular simulation for new low global warming potential refrigerants R1132(E) and R1132a

This study performed surface tension measurements assisted by molecular simulations for new candidate refrigerants R1132(E) and its isomer R1132a, which exhibit extremely low global warming potentials. Because the measured saturation density required for the surface tension measurement by the differential capillary rise method is insufficient at low temperatures, the density data was extrapolated by molecular simulations. In the process, quantum chemical and molecular dynamics simulations were performed to reproduce the vapor–liquid equilibrium state, and the accuracy of the obtained molecular force fields was verified by comparing them with the measured data. Based on the obtained surface tension data, validated temperature correlation equations were proposed for R1132(E) and R1132a, respectively, validated in the temperature range from 209 K to 225 K. Furthermore, their parachors, which relate surface tension to saturation density, were determined from the above data as 116.1 and 116.7 for R1132(E) and R1132a, respectively.

Comparative study on the maximum-pull and tear-off ring method for the measurement of surface tension

The ring method, due to its basic form, is often used in the classroom for an immediate and intuitive grasp of concept of surface tension. Yet, during the measuring process, the large and small results trouble the students. The large values are obtained from the maximum-pull, and the small from the tear-off moment. In this paper, we demonstrate a series of rings with different thicknesses to investigate these two moments. In the water measurement, by subtracting the weight of the liquid raised by the ring or replacing the ring-diameter with tearing-diameter for the moments of maximum pull and film breaking, respectively, a corrected surface tension is obtained. The same correction is also applied in the determination of ethylene glycol and ethanol, but only the moment of maximum pull is applicable. These experimental results are interesting, and will largely stimulate students to understand the concept of surface tension and the ring method of measurement.

Evaluation of surface tensions and root-dentin surface contact angles of different endodontic irrigation solutions

BackgroundSurface tension and contact angle properties, which play a crucial role in determining the effectiveness of irrigation solutions in penetrating dentin surfaces and dentin tubules, are highly important for the development of new irrigation solutions and their preferences. The aim of the current study was to compare the surface tension and contact angle properties of different irrigation solutions used in endodontics, both on the dentin surface and within dentin tubules.MethodsIn this study, the contact angles and surface tensions of 5.25% sodium hypochlorite (NaOCl), 17% ethylenediaminetetraacetic acid (EDTA), 2% chlorhexidine (CHX), 5% boric acid (BA), 0.02% hypochlorous acid (HOCl), 0.2% chlorine dioxide (ClO2), Biopure MTAD, QMix solutions, and distilled water (control group) were measured. Measurements were conducted using a goniometer device (Attension Theta Lite Tensiometer, Biolin Scientific, USA), employing the sessile drop method for contact angle measurements on pre-prepared dentin surfaces, and the pendant drop method for surface tension.ResultsContact angle measurements revealed no statistically significant differences between the contact angle values of MTAD, ClO2, and CHX or between NaOCl, QMix, BA, and HOCl (p > 0.05). However, EDTA exhibited a significantly greater contact angle than did MTAD, ClO2, CHX, NaOCl, QMix, BA, and HOCl (p < 0.05). Furthermore, the contact angle of dentin with distilled water was greater than that with all other solutions tested (p < 0.05). Surface tension measurements revealed that the surface tension values of QMix and MTAD were statistically similar (p > 0.05). CHX exhibited lower surface tension than distilled water and HOCl (p < 0.05), and it also had lower surface tension than ClO2, NaOCl, and BA (p < 0.05). Additionally, the surface tension of the samples treated with EDTA was greater than that of all other solutions tested (p < 0.05).ConclusionThe direct linear relationship between the surface tension of liquids and contact angles on different surfaces may not always hold true, and these values should be considered independently for each solution on various surfaces. Considering the contact angles and surface tension properties of irrigation solutions with root canal dentin, it can be suggested for clinical use that ClO2 could be recommended over NaOCl, and similarly, BA could be recommended over EDTA.

Density Measurements of Molten LiF-BeF2 and LiF-BeF2-LaF3 Salt Mixtures by Neutron Radiography.

The densities of eutectic (LiF)2-BeF2 and mixtures of this salt (FLiBe) with LaF3 were measured by dilatometry and by neutron attenuation from 673 K to 1,073 K. Because LaF3 has a limited solubility in FLiBe, it was necessary to determine the amount of LaF3 in solution before the density could be determined. The FLiBe density determination was favorably benchmarked against the literature data. A simple comparison was not available for the LaF3-FLiBe mixtures, so extrapolation of published data was necessary based on analysis using the Molten Salt Thermal Properties Database-Thermochemistry, or MSTDB-TC, developed by the US Department of Energy. Solubilities for LaF3 in FLiBe ranged from 1 to 4 mol % over 673 to 1,073 K. The salt system was heated and cooled over 24 h to evaluate potential changes in composition and hysteresis during the measurement. Changes in the meniscus were observed, and these were included in the correction for density determinations. Salt surface tension may have led to supersaturation of LaF3 in the salt because the solubility curve was nonlinear with respect to the inverse temperature, as would be expected for an ideal system. Surface tension measurements are currently underway to test this hypothesis.

Interfacial Behavior of Biodegradable Poly(lactic-co-glycolic acid)-Pluronic F127 Nanoparticles and Its Impact on Pickering Emulsion Stability.

Biodegradable nanoparticle-based emulsions exhibit immense potential in various applications, particularly in the pharmaceutical, cosmetic, and food industries. This study delves into the intricate interfacial behavior of Pluronic F127 modified poly(lactic-co-glycolic acid) (PLGA-F127) nanoparticles, a crucial determinant of their ability to stabilize Pickering emulsions. Employing a combination of Langmuir balance, surface tension, and diffusion coefficient measurements, we investigate the interfacial dynamics of PLGA-F127 nanoparticles under varying temperature and ionic strength conditions. Theoretical calculations are employed to elucidate the underlying mechanisms governing these phenomena. Our findings reveal a profound influence of temperature-dependent Pluronic layer behavior and electrostatic and steric interactions on the interfacial dynamics. Nonlinear changes in surface tension are observed, reflecting the interplay of these factors. Particle aggregation is found to be prevalent at elevated temperatures and ionic strengths, compromising the stability and emulsification efficiency of the formed emulsions. This work provides insights into the rational design of stable and efficient biodegradable nanoparticle-based Pickering emulsions, broadening their potential applications in various fields.

Self-assembly of choline-based surface-active ionic liquids and concentration-dependent enhancement in the enzymatic activity of cellulase in aqueous medium.

The micellization of choline-based anionic surface-active ionic liquids (SAILs) having lauroyl sarcosinate [Sar]-, dodecylsulfate [DS]-, and deoxycholate [Doc]- as counter-ions was investigated in an aqueous medium. Density functional theory (DFT) was employed to investigate the net interactional energy (Enet), extent of non-covalent interactions, and band gap of the choline-based SAILs. The critical micelle concentration (cmc) along with various parameters related to the surface adsorption, counter-ion binding (β), and polarity of the cores of the micelles were deduced employing surface tension measurements, conductometric titrations and fluorescence spectroscopy, respectively. A dynamic light scattering (DLS) system equipped with zeta-potential measurement set-up and small-angle neutron scattering (SANS) were used to predict the size, zeta-potential, and morphology, respectively, of the formed micelles. Thermodynamic parameters such as standard Gibb's free energy and standard enthalpy change of micellization were calculated using isothermal titration calorimetry (ITC). Upon comparing with sodium salt analogues, it was established that the micellization was predominantly governed by the extent of hydration of [Cho]+, the head groups of the respective anions, and the degree of counter-ion binding (β). Considering the concentration dependence of the enzyme-SAIL interactions, aqueous solutions of the synthesized SAILs at two different concentrations (below and above the cmc) were utilized as the medium for testing the enzymatic activity of cellulase. The activity of cellulase was found to be ∼7- to ∼13-fold higher compared to that observed in buffers in monomeric solutions of the SAILs and followed the order: [Cho][Sar] > [Cho][DS] > [Cho][Doc]. In the micellar solution, a ∼4- to 5-fold increase in enzymatic activity was observed.

Physicochemical properties of extraction solvents for the advanced recycling of spent nuclear fuel

A comprehensive understanding of solvent physicochemical properties is essential to developing advanced solvent extraction processes, such as Advanced PUREX (Plutonium Uranium Reduction Extraction) and GANEX (Group Actinide Extraction), that can safely and efficiently recycle spent nuclear fuel. The densities, viscosities and surface tensions of binary mixtures of tributyl phosphate (TBP) (0.92–3.66 M) in n-dodecane and N,N-di (2-ethyl hexyl)isobutyramide (DEHiBA) (0.69–2.78 M) in n-dodecane were measured at atmospheric pressure from 278.15 to 333.15 K. Through these measurements, empirical expressions to predict the density and viscosity at any molar composition of these solvents within the studied temperature range were constructed and shown to be in good correlation with all experimental data across the studied variables. The relationship between temperature and viscosity of pure TBP and DEHiBA can be described by the Arrhenius equation for viscosity in the temperature range studied. Surface tension measurements (air-liquid interface) were obtained for varying extractant concentrations between 278.15 and 333.15 K, which showed that DEHiBA acts as a surfactant when mixed with n-dodecane whilst TBP exhibits a higher surface tension than n-dodecane.

A sustainable approach to derive sheep corneal scaffolds from stored slaughterhouse waste.

Aim: The escalating demand for corneal transplants significantly surpasses the available supply. To bridge this gap,we concentrated on ethical and sustainable corneal grafting sources. Our objective was to create viable corneal scaffolds from preserved slaughterhouse waste.Materials & methods: Corneas were extracted and decellularized from eyeballs that had been refrigerated for several days. These scaffolds underwent evaluation through DNA quantification, histological analysis, surface tension measurement, light propagation testing,and tensile strength assessment.Results: Both the native and acellular corneas (with~90% DNA removed using a cost-effective and environmentally friendly surfactant) maintained essential optical and biomechanical properties for potential clinical use.Conclusion: Our method of repurposing slaughterhouse waste, stored at 4°C for several days, to develop corneal scaffolds offers a sustainable and economical alternative xenograft model.

Flowback Additive for Acidizing Fluid to Stimulate Carbonate Gas Reservoirs

Summary Acidizing of oil- and gas-bearing carbonate reservoirs is generally undertaken by using strong mineral acids such as hydrochloric acid (HCl) to enhance permeability. One of the major challenges associated with HCl injection is tuning the reactivity profile to favor the transport of live acid deep into the reservoir while achieving a minimum rock face dissolution. The mineral acid is therefore emulsified in a hydrocarbon phase (e.g., diesel) to retard its reactivity with the rock matrix. The use of emulsified acid is hindered by several limitations such as low emulsion stability at high temperatures, pumping limitations due to high viscosity, the potential of formation damage, and cumbersome mixing procedures at the field scale. In addition, the brines formed as a result of this reaction can be difficult to produce due to higher density and capillary pressures, unfavorable wettability, and low formation pressure. Here, we report on the development of dual-purpose additives that were specifically designed to enhance the recovery of high-density brines and retard the acid/rock reactivity upon addition to the stimulation treatment. Accordingly, seven new additives with fluid flowback properties were developed for use in a single-phase acidizing fluid consisting of HCl (15 wt% and 28 wt%) with the required additives, such as corrosion inhibitor and intensifier, and H2S scavenger. The flowback enhancers (FBEs) were formulated from a blend of water, ester or terpene solvents, alcohols, and surfactants to form optically clear nano- and microemulsions. Surfactant selection was driven by the need to exhibit demulsification properties with condensate, high chemical and thermal stability, compatibility in strongly acidic media, and high-density brines under harsh reservoir conditions. To assess the FBE performance in acidizing formulations (i.e., to serve as both an FBE and retarder), screening studies consisting of static rock dissolution tests and surface tension measurements were performed to downselect FBEs suitable for this application. This was coupled with brine displacement tests in addition to compatibility and stability studies. FBEs that demonstrated superior performance were then selected for further evaluation under reservoir conditions [i.e., core flow matrix acidizing to measure regained permeability and computed tomography (CT) scan for analyzing the wormhole propagation]. The droplet size of the as-prepared nano- and microemulsions was found to be between 10 nm and 850 nm. The FBEs formulated in this study were found to prevent emulsion formation in the presence of condensate and demonstrated remarkable chemical and thermal stability in concentrated acid at temperatures up to 300°F for a duration of up to 24 hours, as confirmed by the consistent low surface tension values (21–29 mN/m). With regard to fluid displacement, column tests performed under ambient conditions revealed quick brine displacement with recovery exceeding 75 vol% in comparison with 16 vol% in the absence of the FBE. Interestingly, the addition of a select FBE from this study to 28 wt% HCl was found to retard the reaction of carbonate dissolution at room temperature. This led us to assess the performance under reservoir conditions utilizing core flow testing. Accordingly, the addition of FBE-F to 28 wt% HCl led to an improvement in permeability by up to 267% as compared with 15% without FBE added. These results are further supported by the CT scan images of the acidized cores, which revealed the formation of a deeper wormhole in the presence of a select FBE.