Nonionic Mixed Surfactant Stabilized Water-in-Oil Microemulsions for Active Ingredient In Vitro Sustained Release

Olive oil is an excellent dispersing medium for water‐in‐oil microemulsions as it helps hydrate the skin and enhances the release of the active ingredients. In this study, mixed surfactants containing Span^® 80 with varied Tween^® series at 1:1 ratio were prepared with olive oil and water to produce water‐in‐oil microemulsions. The microemulsions were used to study the in vitro release of the active ingredients with different water solubilities. A microemulsion olive oil/water/mixed surfactant (56:4:40 by weight) was selected from the constructed phase diagram for further physical characterization. The analysis showed that the microemulsion composed of Span^® 80 and Tween^® 80 (ST80) was the most suitable surfactant combination. Equal amounts of ascorbic acid, caffeine and lidocaine were solubilized in ST80 microemulsions to study their release rate. Physical evaluation of ST80 microemulsions incorporating the active ingredients showed no apparent change compared to the ST80 microemulsion alone. The in vitro release study showed that the rate of active ingredients released from the microemulsion into the receptor chamber depends on their hydrophobicity, whereby lidocaine and caffeine were fivefold and twice as fast, respectively, with respect to ascorbic acid. ST80 microemulsions show constant rate of active ingredient release, demonstrating the sustained release properties of the system.     

The Impact of Polyoxyethylene Sorbitan Surfactants in the Microstructure and Rheological Behaviour of Emulsions Made With Melted Fat From Cupuassu (<Emphasis Type="Italic">Theobroma grandiflorum</Emphasis>)

Cupuassu fat is a good candidate for partial substitution of cocoa butter in many products, including emulsions. However, for such use it is necessary to know the characteristics of the products prepared with cupuassu fat. Therefore, the main goal of this work is to characterize emulsions prepared with cupuassu fat using the surfactants Tween^® 60, Tween^® 80 and Tween^® 85 as emulsifiers. The emulsions were prepared at 43 °C with addition of 0.5 or 1.5 % (w/v) of surfactant and compared with an emulsion without surfactant. All emulsions were analysed by conductivity, stability, pH, optical microscopy, rheology and oxidative stability. It was verified that the emulsions prepared with Tween^® 60 and Tween^® 80 have higher stability, smaller droplet size and higher apparent viscosity. Also, these properties are positively influenced by the concentration of the surfactant. On the other hand, emulsions prepared with Tween 85 or without surfactant reached unsatisfactory results. The rheological behaviour of the emulsions was adequately described by both Herschel-Bulkley and Mizhari-Berki models revealing pseudoplastic character. These emulsions also present strong gel behaviour, with storage modulus higher than loss modulus. In conclusion, cupuassu fat can be used as oil phase for emulsions products and this characterization helps to understand their behaviour in order to increase their use in food industry.     

Insight into the Interaction Between Carbopol® 940 and Ionic/Nonionic Surfactant

Mixtures of a cross‐linked polyacrylic acid (Carbopol^® 940) and two types of surfactants, namely anionic sodium dodecylsulfate (SDS) and nonionic Tween^® 80, were investigated by viscometry, conductometry, tensiometry, spectrophotometry, fluorimetry and scanning electron microscopy (SEM). The addition of nonionic surfactant decreased the reduced viscosity and the transmittance of the Carbopol^® polymer aqueous solutions. Furthermore, the interaction between Carbopol^® 940 and SDS was characterized by two significant concentration values: the critical aggregation concentration of SDS was particularly independent of Carbopol^® polymer concentration while the polymer saturation point of both surfactants increased with the increase in polymer content. The values of critical aggregation concentration and polymer saturation point obtained using various techniques confirmed the occurrence of Carbopol^® polymer–surfactant associations. The effect of different SDS and Tween^® 80 concentrations on the conformation of Carbopol^® 940 in aqueous solution could be explained through hydrophobic association between surfactant micelles and Carbopol^® polymer tails and through hydrogen bonding in the case of Tween^® 80. Additionally, the surfactant‐induced structural changes were confirmed in Carbopol^® 940–SDS and Carbopol^® 940–Tween^® 80 aqueous solutions by SEM measurements.     

Methods of Emulsifying Linoleic Acid in Biohydrogenation Studies In Vitro May Bias the Resulting Fatty Acid Profiles

The effects of three emulsifying methods on ruminal fatty acid biohydrogenation (BH) in vitro were compared. Using a static in-vitro gas test system, four replicates of each treatment were incubated in buffered ruminal fluid. Hemicellulose (300 mg dry matter) was supplemented either with or without linoleic acid (9c12c-18:2, 5% in diet dry matter) and incubated for 4 and 24 h. Three methods of emulsifying 9c12c-18:2 were tested: (1) ethanol, (2) Tween^® 80, and (3) sonication. The products were then compared to non-emulsified 9c12c-18:2. Out of the three emulsifying methods tested, ethanol and sonication resulted in stable 9c12c-18:2 emulsions, indicating good 9c12c-18:2 distribution, while the Tween^® 80 emulsion was less stable. BH was strongly inhibited by treating 9c12c-18:2 with ethanol and sonication at different steps of the BH-pathway, resulting in changed concentrations of certain BH intermediates. The fatty acid profile generated from the major BH-pathways of 9c12c-18:2 with Tween^® 80 was comparable to that without emulsification after 24 h of incubation. We conclude that it is not recommended to emulsify lipids before incubating them in vitro when investigating fatty acid BH. If emulsification of 9c12c-18:2 is necessary, Tween^® 80 seems to be the method that interferes least with BH.     

Viscoelastic Surfactants with High Salt Tolerance,Fast‐Dissolving Property,and Ultralow Interfacial Tension for Chemical Flooding in Offshore Oilfields

Injected chemical flooding systems with high salinity tolerance and fast‐dissolving performance are specially required for enhancing oil recovery in offshore oilfields. In this work, a new type of viscoelastic‐surfactant (VES) solution, which meets these criteria, was prepared by simply mixing the zwitterionic surfactant N‐hexadecyl‐N,N‐dimethyl‐3‐ammonio‐1‐propane sulfonate (HDPS) or N‐octyldecyl‐N,N‐dimethyl‐3‐ammonio‐1‐propane sulfonate (ODPS) with anionic surfactants such as sodium dodecyl sulfate (SDS). Various properties of the surfactant system, including viscoelasticity, dissolution properties, reduction of oil/water interfacial tension (IFT), and oil‐displacement efficiency of the mixed surfactant system, have been studied systematically. A rheology study proves that at high salinity, 0.73 wt.% HDPS/SDS‐ and 0.39 wt.% ODPS/SDS‐mixed surfactant systems formed worm‐like micelles with viscosity reaching 42.3 and 23.8 mPa s at a shear rate of 6 s^?1, respectively. Additionally, the HDPS/SDS and ODPS/SDS surfactant mixtures also exhibit a fast‐dissolving property (dissolution time <25 min) in brine. More importantly, those surfactant mixtures can significantly reduce the IFT of oil–water interfaces. As an example, the minimum of dynamic‐IFT (IFT_min) could reach 1.17 × 10^?2 mN m^?1 between the Bohai Oilfield crude oil and 0.39 wt.% ODPS/SDS solution. Another interesting finding is that polyelectrolytes such as sodium of polyepoxysuccinic acid can be used as a regulator for adjusting IFT_min to an ultralow level (<10^?2 mN m^?1). Taking advantage of the mobility control and reducing the oil/water IFT of those surfactant mixtures, the VES flooding demonstrates excellent oil‐displacement efficiency, which is close to that of polymer/surfactant flooding or polymer/surfactant/alkali flooding. Our work provides a new type of VES flooding system with excellent performances for chemical flooding in offshore oilfields.     

Preparation and Performance Evaluation of Fatty Amine Polyoxyethylene Ether Diethyl Disulfonate for Enhanced Oil Recovery in High‐Temperature and High‐Salinity Reservoirs

To enhance oil recovery in high‐temperature and high‐salinity reservoirs, a novel fatty amine polyoxyethylene ether diethyl disulfonate (FPDD) surfactant with excellent interfacial properties was synthesized. The interfacial tension (IFT) and contact angle at high temperature and high salinity were systematically investigated using an interface tension meter and a contact angle meter. According to the experimental results, the IFT between crude oil and high‐salinity brine water could reach an ultra‐low value of 10^?3 mN m^?1 without the aid of extra alkali at 90°C after aging. The FPDD surfactant has strong wettability alternation ability that shifts wettability from oil‐wet to water‐wet. The FPDD surfactant with a high concentration also has good emulsion ability under high‐temperature and high‐salinity conditions. Through this research work, we expect to fill the lack of surfactants for high‐temperature and high‐salinity reservoirs and broaden its great potential application area in enhanced oil recovery.     

Microemulsion formation and detergency with oily soils: II. Detergency formulation and performance

In part I of this series (J. Surfact. Deterg. 6, 191–203, 2003), the mixed surfactant system of sodium dioctyl sulfosuccinate (AOT), alkyl diphenyl oxide disulfonate (ADPODS) and sorbitan monooleate (Span 80) was shown to form Winsor type I and type III microemulsions with hexadecane and motor oil. In addition, high solubilization and low interfacial tension were obtained between the oils and surfactant solutions both in the supersolubilization region (Winsor type I system close to type III system) and at optimal conditions in a type III system. In the present study, this mixed surfactant system was applied to remove oily soil from fabric (a polyester/cotton blend), and detergency results were correlated to phase behavior. Dynamic interfacial tensions were also measured between the oils and washing solutions. In the supersolubilization and in the middle-phase regions (type III), much better detergency performance was found for both hexadecane and motor oil removal than that with a commercial liquid detergent product. In addition, the detergency performance of our system at low temperature (25°C) was close to that obtained at high temperature (55°C), consistent with the temperature robustness of the microemulsion phase behavior of this system.     

Novel fluorinated surfactants for enhanced oil recovery in carbonate reservoirs

Novel surfactant‐polymer (SP) formulations containing fluorinated amphoteric surfactant (surfactant‐A) and fluorinated anionic surfactant (surfactant‐B) with partially hydrolyzed polyacrylamide (HPAM) were evaluated for enhanced oil recovery applications in carbonate reservoirs. Thermal stability, rheological properties, interfacial tension, and adsorption on the mineral surface were measured. The effects of the surfactant type, surfactant concentration, temperature, and salinity on the rheological properties of the SP systems were examined. Both surfactants were found to be thermally stable at a high temperature (90 °C). Surfactant‐B decreased the viscosity and the storage modulus of the HPAM. Surfactant‐A had no influence on the rheological properties of the HPAM. Surfactant‐A showed complete solubility and thermal stability in seawater at 90 °C. Only surfactant‐A was used in adsorption, interfacial tension, and core flooding experiments, since surfactant‐B was not completely soluble in seawater and therefore was limited to deionized water. A decrease in oil/water interfacial tension (IFT) of almost one order of magnitude was observed when adding surfactant‐A. However, betaine‐based co‐surfactant reduced the IFT to 10^?3 mN/m. An adsorption isotherm showed that the maximum adsorption of surfactant‐A was 1 mg per g of rock. Core flooding experiments showed 42 % additional oil recovery using 2.5 g/L (2500 ppm) HPAM and 0.001 g/g (0.1 mass%) amphoteric surfactant at 90 °C.     

Optimization of Phospholipid Nanoparticle Formulations Using Response Surface Methodology

The present study deals with the optimization of phospholipid liposome formulations to mimic red blood cells. Optimization of different concentrations of distearylphosphatidylcholine, dipalmitoylphosphatidylcholine, and phosphatidylserine at a fixed concentration of lecithin and Tween^® 80 was done using response surface methodology. The optimized formulation produced liposomes with a particle size in the range of 112–196 nm. The optimized formulation shows low encapsulation efficiency at low levels of insulin but increases at higher loading levels. Formulated vesicles fulfill the size requirement for intravenous drug delivery. The present system is environmentally friendly with respect to biodegradability and biocompatibility.     

The Effects of Dynamic Noncovalent Interaction between Surfactants and Additional Salt on the pH-Switchable Interfacial Tension Variations

The dynamic noncovalent interaction between the anionic surfactant sodium dodecyl benzene sulfonate (SDBS) and 1,3-diphenylguanidine (DPG) was employed to control the interfacial activity of the surfactant. At high HCl concentration (1000 mg L⁻¹), the SDBS/DPGⁿ⁺ system could reduce the water/oil interfacial tension (IFT) to 10⁻⁴ mN m⁻¹ order of magnitude, which was much lower than the IFT values in the SDBS/DPG⁺ system with a low HCl concentration (100 mg L⁻¹) and the individual SDBS system by three and four orders of magnitude, respectively. The pH-switchable protonation of amido groups in DPG molecules determines the SDBS/DPG molecular interaction and the amplitude of IFT reduction, which was confirmed by control experiments using two other surfactants (sodium dodecyl sulfate [SDS] and dodecyl trimethylammonium bromide [DTAB]). Moreover, the investigation of the NaCl and temperature effects on the IFT indicated the intensity of mixed SDBS/DPGⁿ⁺ adsorption layers at the water/oil interface.     

Formation and stabilization of submicron particles via rapid expansion processes

Submicron particles were produced by rapid expansion of supercritical solution into air (RESS) or an aqueous surfactant solution (RESSAS) to minimize particle growth and to prevent particle agglomeration. Thereby the effect of process conditions on the size of the particles precipitated was investigated. The obtained product was evaluated by measuring particle size by 3-wavelength extinction measurements, dynamic light scattering, specific surface areas by nitrogen gas adsorption, melting behaviour by differential scanning calorimetry, particle morphology by X-ray diffraction, scanning electron micrographs (SEM), and drug loading by high performance liquid chromatography.Prior to the particle formation experiments, the melting temperature of Salicylic acid under CO₂ pressure and the solubility of Salicylic acid in CO₂ were measured. The size of Salicylic acid particles produced via RESS decreased from 230 to 130 nm as the pre-expansion temperature decreased from 388 to 328 K and the specific surface area of the micronized particles was found to be up to 60 times higher than that of the unprocessed material. RESSAS experiments demonstrate that in 1 wt.% Tween 80 solutions Salicylic acid concentrations of 4.6 g/dm³ could be stabilized with particle diameters in the range of 180 nm. Additional experiments show that Ibuprofen nanoparticles with an average size of 80 nm and a drug concentration of 2.4 g/dm³ could be stabilized in 1 wt.% Tween^® 80 solutions. The use of a SDS solution instead of Tween^® 80 results in a stable aqueous suspension of phytosterol nanoparticles, where the average particle size is 50 nm at a drug concentration of 5.6 g/dm³.     

A Star-Shaped Anionic Surfactant: Synthesis,Alkalinity Resistance,Interfacial Tension and Emulsification Properties at the Crude Oil–Water Interface

In this research, a star‐shaped surfactant was synthesized through the chlorination reaction, alkylation reaction and sulfonation reaction of triethanolamine, which is composed of three hydrophobic chains and three sulfonate hydrophilic groups. The critical micelle concentration (CMC) of the surfactant was measured by the surface tension method, and the results showed that it had high surface activity with CMC of 5.53 × 10^?5 mol/L. The surfactant was superior in surface active properties to the reference surfactants SDBS and DADS‐C₁₂. The interfacial tension (IFT) of the studied crude oil–water system (surfactant concentration 0.1 g/L, NaOH concentration 0.5 g/L, and experimental temperature 50 °C) dropped to 1.1 × 10^?4 mN/m, which can fulfil the requirement of surfactants for oil displacement. An aqueous solution of the surfactant and crude oil was emulsified by shaking, which formed a highly stable oil‐in‐water (O/W) emulsion with particle size of 5–20 μm. The oil displacement effect was almost 12%.     

Novel alkyl methylnaphthalene sulfonate surfactants: A good candidate for enhanced oil recovery

The surface tensions of various surfactant aqueous solution and the dynamic interfacial tensions between the Shengli oil field of China crude oil and the solution of novel surfactants, a series of single-component alkylmethylnaphthalene sulfonates (AMNS) including various the length of alkyl chains (hexyl, octyl, decyl, dodecyl and tetradecyl, developed in our laboratory), were measured. It is found that synthesized surfactants exhibited great capability and efficiency of lowering the solution surface tension. The critical micelle concentrations, CMC were: 6.1–0.018×10⁻³ mol L⁻¹, and the surface tensions at CMC, γ_CMC were: 28.27–35.06 mN m⁻¹. It is also found that the added surfactants are greatly effective in reducing the interfacial tensions and can reduce the tensions of oil–water interface to ultra-low, even 10⁻⁶ mN m⁻¹ at very low surfactant concentration without alkali. The addition of salt, sodium chloride, results in more effectiveness of surfactant in reducing interfacial tension and shows that there exist obviously both synergism and antagonism between the surfactant and inorganic salt. All of the synthesized surfactants, except for hexyl methylnaphthalene sulfonate, can reduce the interfacial tension to ultra-low at an optimum surfactant concentration and salinity. Especially Tetradec-MNS surfactant is most efficient on lowering interfacial tension between oil and water without alkaline and the other additives at a 0.002 mass% of very low surfactant concentration. Both chromatogram separation of flooding and breakage of stratum are avoided effectively, in addition to the less expensive cost for enhanced oil recovery, and therefore it is a good candidate for enhanced oil recovery.     

Biodesulphurisation of Dibenzothiophene in Hydrophobic Media by Rhodococcus sp. Strain IGTS8

Rhodococcus sp. strain IGTS8 (ATCC 53968) is capable of removing organic sulphur from various organosulphur compounds such as dibenzothiophene (DBT). Since substrates for this process are invariably hydrophobic, parameters of the biodesulphurisation of DBT in hydrophobic systems were examined. Freeze-dried bacteria, stored for 3 months at -80°C with negligible loss of activity were used primarily as biocatalysts. The most efficacious order of ingredient addition was with oil and water (plus surfactant if used) mixed first and then freeze-dried bacteria added. Various oil/water ratios were examined. The minimum water requirement for desulphurisation was 1·25 cm³ g⁻¹ dry weight. If the minimum water requirement was met, biodesulphurisation at an 90% oil/water (w/w) ratio was still 82% of the maximum at an 80% oil/water ratio. The surfactants, oleic diethanolamine and Triton N101, both stimulated biodesulphurisation in oil/water systems but not in 100% water. The desulphurisation of DBT in oil/water emulsions persisted for 8–16 h, but the rate rapidly declined after 3 h; biodesulphurisation in aqueous media stopped after 3–4 h. © 1997 SCI.     

Enhanced oil recovery from high‐salinity reservoirs by cationic gemini surfactants

In order to enhance oil recovery from high‐salinity reservoirs, a series of cationic gemini surfactants with different hydrophobic tails were synthesized. The surfactants were characterized by elemental analysis, infrared spectroscopy, mass spectrometry, and ¹H‐NMR. According to the requirements of surfactants used in enhanced oil recovery technology, physicochemical properties including surface tension, critical micelle concentration (CMC), contact angle, oil/water interfacial tension, and compatibility with formation water were fully studied. All cationic gemini surfactants have significant impact on the wettability of the oil‐wet surface, and the contact angle decreased remarkably from 98° to 33° after adding the gemini surfactant BA‐14. Under the condition of solution salinity of 65,430 mg/L, the cationic gemini surfactant BA‐14 reduces the interfacial tension to 10^?3 mN/m. Other related tests, including salt tolerance, adsorption, and flooding experiments, have been done. The concentration of 0.1% BA‐14 remains transparent with 120 g/L salinity at 50 °C. The adsorption capacity of BA‐14 is 6.3–11.5 mg/g. The gemini surfactant BA‐14 can improve the oil displacement efficiency by 11.09%. © 2017 Wiley Periodicals, Inc. J. Appl. Polym. Sci. 2018 , 135, 46086.     

Effect of UV Processing Treatments on Soy Oil Conjugated Linoleic Acid Yields and Tocopherols Stability

Photoirradiation has been used to synthesize 20 % conjugated linoleic acid (CLA) in soy oil with an iodine catalyst. CLA yields are affected by ultraviolet (UV) irradiation time, Magnesol^® adsorbent treatment, iodine concentration and mixed tocopherols. However, these factors in combination had not been studied. Therefore, the objectives of this study were to determine the effect of (1) a combination of photoirradiation time, Magnesol^® adsorbent treatment and added mixed soy tocopherols on CLA yields and the oxidative stability of CLA-rich soy oil, (2) UV light on mixed tocopherol stability, as tocopherols enhance CLA yields during photoirradiation. Soy oil was initially treated with 5 % Magnesol^®. Iodine at 0 and 0.35 % was mixed with Magnesol^®-treated soy oil and irradiated for 12 and 6 h. The irradiated oil was again treated with Magnesol^®, mixed with 0, 0.35 or 0.175 % iodine; 1400 MT and irradiated for 12 or 6 more hours. CLA content in soy oil was determined by conventional gas chromatography-flame ionization detector. The oxidative stability of the oil was determined by measuring peroxide value (PV). The tocopherols stability was determined by high performance liquid chromatography. The results showed that increasing photoirradiation time increased CLA yields and lowered PV. Magnesol^® adsorption produced highest CLA yield for all treatments by removing peroxides in RBD soy oil. The γ-tocopherols exhibited highest stability during UV irradiation. The order of tocopherol degradation was α-tocopherol > δ-tocopherol > γ-tocopherols.     

Effect of surfactant additives on co-current gas-liquid downflow

The influence of a surfactant additive on the interfacial structure and on the transition from the smooth to the wavy stratified flow regime in inclined pipes is investigated for various gas-liquid flow rates. The effect of a surfactant on the gas-liquid stratified downflow patterns is studied using a dilute aqueous solution of a non-ionic surfactant (Tween^®80), which is found to have a dramatic effect on two-phase flow characteristics. A conventional solution having a surface tension similar to that of the surfactant solution is also employed and this verifies that the atypical behavior of the surfactant solution is ascribed to its special chemical structure and not to its low surface tension. Liquid layer thickness time records are acquired using a parallel-wire conductance technique from which the statistics of the layer thickness, as well as wave celerities, are calculated. Laser doppler anemometry (LDA) is employed to investigate the flow structure in the thin liquid layer both with and without interfacial shear induced by a co-current gas flow. A differential pressure transducer is used for pressure drop measurements in the liquid phase. The interpretation of the results verifies that the “delayed” appearance of the interfacial waves should be associated with the turbulence retardation within the liquid layer and it facilitates the clarification of the mechanisms in which the surfactant interacts with the turbulent structures and causes significant drag reduction.     

Interfacial tension behavior of athabasca bitumen/aqueous surfactant systems

The spinning drop method was used to measure the interfacial tension of Athabasca bitumen in contact with an aqueous phase (D₂O); variables included temperature, salinity, alkalinity, surfactant type (TRS 10–80, Suntech 5, sodium dodecyl sulfate), surfactant concentration, isopropyl alcohol concentration, bitumen drop size and age of interface. In the absence of surfactant, the bitumen/aqueous interfacial tension decreased with increasing temperature and salinity. Bitumen drops contacting alkaline medium exhibited interfacial tension minima below a pOH of three. In the presence of surfactant, the interfacial tension behavior was often complex. The interfacial tension-concentration plot for Suntech 5 surfactant exhibited two CMC type discontinuities. Low interfacial tension (<0.01 mN m^?1) was observed only in the presence of added electrolyte. Interfacial tension values were sensitive to the age of surfactant preparation and volume ratio of the oleic-to-aqueous phases. The interfacial tension of the bitumen/brine-TRS 10–80 system increased upon addition of isopropyl alcohol. An increase in temperature required an increase in salinity to maintain a constant low interfacial tension. The experimental results are discussed in terms of changes in the structure of the amphiphile at the bitumen/aqueous interface.     

Surfactant (in situ)–Surfactant (Synthetic) Interaction in Na2CO3/Surfactant/Acidic Oil Systems for Enhanced Oil Recovery: Its Contribution to Dynamic Interfacial Tension Behavior

The effect of synthetic surfactant molecular structure on the dynamic interfacial tension (DIFT) behavior in Na₂CO₃/surfactant/crude oil was investigated. Three surfactants, a nonionic (iC₁₇(EO)₁₃), an alcohol propoxy sulfate (C_14–15(PO)₈SO₄), and sodium dodecyl sulfate (SDS) were considered in this study. Sodium tripolyphosphate (STPP) was added to ensure complete compatibility between brine and Na₂CO₃. In Na₂CO₃/iC₁₇(EO)₁₃/oil and Na₂CO₃/C_14–15(PO)₈SO₄/oil systems, a strong synergistic effect for lowering the dynamic interfacial tension was observed, in which the dynamic IFT are initially reduced to ultralow transient minima in the range 1.1 × 10^?3–6.6 × 10^?3 mNm^?1 followed by an increment to a practically similar equilibrium value of 0.22 mNm^?1 independent of Na₂CO₃ concentration (for iC₁₇(EO)₁₃) and to decreasing equilibrium values with increasing alkali concentrations (for C_14–15(PO)₈SO₄). The observed difference in the equilibrium IFT for the two systems suggest that in both systems, the mixed interfacial film is efficient in reducing the dynamic interfacial tension to ultralow transient minima (～10^?3 mNm^?1) but the mixed film soap‐iC₁₇(EO)₁₃ is much less efficient than the mixed film soap‐C_14–15(PO)₈SO₄ in resisting soap diffusion from the interface to the bulk phases. In both systems, the synergism was attributed, in part, to the intermolecular and intramolecular ion–dipole interactions between the soap molecules and the synthetic surfactant as well as to some shielding effect of the electrostatic repulsion between the carboxylate groups by the nearby ethylene oxide (13 EO) and propylene oxide (8 PO) groups in the mixed interfacial monolayer. SDS surfactant showed a much lower synergism relative to iC₁₇(EO)₁₃ and C_14–15(PO)₈SO₄, probably due to the absence of ion–dipole interactions and shielding effect in the mixed interfacial layer at the oil–water interface.     

A New Benzylated Fatty Acid Amide Amphoteric Surfactant Derived from Hydrogenated Castor Oil with Ultra-Low Interfacial Tension between Crude Oil and Brine

Hydrogenated castor oil from castor oil is promisingly used as raw materials for lubricants, coatings, cosmetics, and pharmaceutics due to high melting point and stable physical properties. However, the chemical modification of the hydrogenated castor oil has been rarely investigated. Here, we report a N-phenyl-fatty-amido-1-propyl-N,N-dimethyl-amino-carboxyl-betaine surfactant derived from hydrogenated castor oil with excellent interfacial properties through a rapid synthetic process, including direct alkylation, amidation, and quaternization. The interfacial tension between crude oil and brine was ultra-low for a low dosage of 0.007 g L⁻¹ of surfactant in aqueous solution without any alkali addition, which implies a potential application in enhanced oil recovery.