Surfactant Concentration Research Articles

Influence of various surfactants on the stability and solidification characteristics of DI water-based CuO NFPCM for cool thermal energy storage system

The current study goals to investigate the stability and solidification characteristics of deionized water (DI water) based copper oxide (CuO) nanofluid phase change materials (NFPCMs) with a nucleating agent, different types of surfactants (SBDS, CTAB, and GA) and different weight concentration of surfactant for cool thermal energy storage systems (CTES). The stability of NFPCMs was assessed through average particle size distribution, zeta potential, and UV–vis absorbance. Among all NFPCMs, 0.1 wt% SDBS - CuO NFPCM showed prolonged stability with −42.7 mV and 212.6 nm of zeta potential and average particle size value. The heat transfer properties of NFPCMs were studied with differential scanning calorimetry (DSC), Thermogravimetric analysis (TGA) and thermal conductivity measurements. The introduction of 0.05 wt% SDBS to NFPCM resulted in a notable 17.84 % and 7.64 % increase in thermal conductivity in solid and liquid states, with a slight decrease in latent heat by 5.2 % and 6.01 % during melting and crystallization as compared to DI water. The solidification experiments of NFPCMs were investigated in a spherical encapsulation at a surrounding bath temperature of −8 °C and − 10 °C. Comparing various surfactants in NFPCMs, the SDBS–CuO NFPCM was the most efficient in reducing the solidification time by 26.3 % and 28.4 % at −8 °C and − 10 °C respectively, compared to the nucleating agent PCM (NAPCM). Further, the different concentrations of SDBS in NFPCM demonstrated that 0.05 wt% SDBS–CuO NFPCM displayed the greatest reduction in solidification time, achieving 29.4 % and 27.7 % at −10 °C and − 8 °C, respectively, compared to the NAPCM.

Molecular simulation of the effect of anionic surfactant on methane diffusion in coal

Coal seam water injection is one of the important means of coal mine disaster prevention and control, which helps to reduce gas concentration. Anionic surfactants can change the hydrophilicity of coal to enhance the wetting effect of coal seam water injection and inhibit the diffusion of methane. However, the research on the effect of surfactants on the diffusion process of methane is still relatively weak. In order to explore the influence mechanism of anionic surfactant on coal surface wettability and methane diffusion from a microscopic point of view. Using wiser coal model and two commonly used anionic surfactants, sodium dodecyl benzene sulfonate (SDBS) and sodium dodecyl sulfate (SDS), the surfactant/water interface configuration, water/coal contact angle configuration and coal seam methane diffusion configuration were constructed. The interfacial stability of surfactant and water was discussed, and the wetting modification effect of surfactant on coal surface and the law of gas diffusion were analyzed. Finally, by studying the microscopic properties of each molecule in the simulation system, the adsorption mode of surfactants, the hydrophilicity of polar groups, the number of hydrogen bonds and the change of the pore volume in the coal seam system were analyzed, and the wetting modification mechanism of surfactants on coal surface and the inhibition effect of methane diffusion were discussed. The results show that with the increase of surfactant concentration, the interface formation energy is constantly enhanced, and the absolute value of electrostatic energy gradually increases, making the effect between surfactant and water stronger. The contact angle of coal surface under the action of SDS surfactant is the smallest, which is 36.230°, indicating that SDS surfactant has the best effect on the wettability of coal surface. The amount of methane diffusion in the surfactant action system decreased significantly compared with the pure water system, and the distribution of methane in the coal seam increased, indicating that the interaction between methane and coal is enhanced under the action of surfactant. With the increase of surfactant concentration, surfactant molecules are easier to spread on the surface of coal seam, and the wettability of coal surface increases. The research results can provide some research ideas and reference significance for anionic surfactants in the prevention and control of coal mine gas disasters.

Comprehensive Evaluation of Tilted Fiber Bragg Grating (TFBG) Sensors for Characterizing Oil–Water Emulsions: A Study on the Impact of Surfactant Concentration and Mixing Speed

Comprehensive Evaluation of Tilted Fiber Bragg Grating (TFBG) Sensors for Characterizing Oil–Water Emulsions: A Study on the Impact of Surfactant Concentration and Mixing Speed

Innovative stearic acid-in-silicone oil (o/o) phase change material lubricating emulsions (PCMLEs): Thermo-rheological and tribological properties

This paper analyses the feasibility of using novel non-aqueous stearic acid-in-silicone oil (o/o) phase change material lubricating emulsions (PCMLEs). The novel use of these dispersions with heat storage capacity for lubricating applications can be considered a new approach since they have not yet been used for such purposes. In this study, PCMLEs consist of stearic acid, with a melting point of roughly 69 °C, as a dispersed phase change material in a continuous silicone oil medium. Samples were prepared by mixing different phase ratios, by high-shear processing and stabilised by a constant concentration of a silicone-based non-ionic surfactant. Taking into consideration the ability of stearic acid to absorb latent thermal energy during machinery operation, the potential application in lubrication has been assessed by means of stationary and temperature ramp friction tests. Moreover, the effect of the phase transition on the PCMLEs’ rheological response has been analysed through stationary flow tests and frequency sweeps within the linear viscoelastic range at constant temperatures, below (40 °C) and above (80 °C) the melting process of the disperse phase. Additionally, their thermal properties and morphology were also studied through X-ray diffraction measurements (XRD), differential scanning calorimetry (DSC) and polarised optical microscopy. As a result, the reported rheological properties and microstructure led to the enhancement in tribological characteristics of PCMLEs since a significant reduction in the friction factor is evidenced, within the whole temperature range, when compared to the silicone oil.

Pulmonary surfactant impacts in vitro activity of selected antifungal drugs against Candida krusei and Candida albicans

PurposeThis study investigates how surfactants affect the in-vitro anti-infective efficacy of micafungin, caspofungin, anidulafungin, and amphotericin B in treating pulmonary mycoses.MethodsMIC values for antifungal agents were determined against Candida krusei (now Pichia kudriavzevii) ATCC 6258, Candida albicans ATCC 90028, and 18 clinical isolates using the broth microdilution method in RPMI medium, following EUCAST recommendations. MIC assays included testing with and without Curosurf® surfactant at 1 mg/mL for C. krusei ATCC 6258 and all C. krusei isolates. Subsequent Time-kill studies in Sabouraud broth involved testing both C. albicans ATCC 90028 and C. krusei ATCC 6258 strains at concentrations equal their respective MIC values, with and without surfactant, using all four antifungals. CFU/mL were assessed at multiple time points up to 24 h. TKCs with different surfactant concentrations for C. krusei ATCC 6258 and mini-TKCs at various concentrations relative to the MIC of C. krusei isolates and the reference strain were conducted with micafungin, anidulafungin, and caspofungin.ResultsMIC results showed that 1 µg/mL surfactant reduced killing of micafungin and anidulafungin against C. krusei, while caspofungin was unaffected. Amphotericin B's MIC decreased by half. TKCs demonstrated significant effects of surfactant on micafungin and anidulafungin against C. krusei, with complete abolition of anidulafungin's activity against C. albicans.ConclusionThis in-vitro study highlights the concentration-dependent inhibitory effect of surfactant on antifungal activity against C. krusei and, to some extent, C. albicans, necessitating further clinical validation for invasive lung mycoses treatment.

Charge Regulation at the Nanoscale as Evidenced from Light-Responsive Nanoemulsions.

Emulsions are indispensable in everyday life, and the demand for emulsions' diversity and control of properties is therefore substantial. As emulsions possess a high internal surface area, an understanding of the oil/water (o/w) interfaces at the molecular level is fundamental but often impaired by experimental limitations to probe emulsion interfaces in situ. Here, we have used light-responsive surfactants (butyl-AAP) that can photoisomerize between E and Z isomers by visible and UV light irradiation to tune the emulsion interfaces. This causes massive changes in the interface tension at the extended o/w interfaces in macroemulsions and a drastic shift in the surfactants' critical micelle concentration, which we show can be used to control both the stability and phase separation. Strikingly different from macroemulsions are nanoemulsions (RH ∼90 nm) as these are not susceptible to E/Z photoisomerization of the surfactants in terms of changes in their droplet size or ζ-potential. However, in situ second-harmonic scattering and pulsed-field gradient nuclear magnetic resonance (NMR) experiments show dramatic and reversible changes in the surface excess of surfactants at the nanoscopic interfaces. The apparent differences in ζ-potentials and surface excess provide evidence for a fixed charge to particle size ratio and the need for counterion condensation to renormalize the particle charge to a critical charge, which is markedly different compared to the behavior of very large particles in macroemulsions. Thus, our findings may have broader implications as the electrostatic stabilization of nanoparticles requires much lower surfactant concentrations, allowing for a more sustainable use of surfactants.

Optimisation of microencapsulation efficiency of propolis phenolic compounds by double emulsion method using response surface methodology

AbstractThe aim of this study was to optimise the microencapsulation efficiency of propolis phenolic compounds by double emulsion solvent evaporation technique (W1/O/W2). The solvent/sample ratio and the polymer and surfactant concentration parameters were optimised using response surface methodology (RSM) through Box–Behnken Design (BBD). For each parameter studied, total phenolic content encapsulation efficiency (TPCEE), free radical scavenging activity (DPPH), and ferric reducing antioxidant power (FRAP) were evaluated. The results showed that the optimal parameters were: 31.60 mg mL−1 for sample/solvent ratio, 606.28 mg mL−1 for poly(ε-caprolactone) (PCL) concentrations, and 2.05 g mL−1 for poly(vinyl alcohol) (PVA) concentration. The optimum values obtained were: 84.62% for encapsulation efficiency of phenolic content, 51.89% for DPPH, and 48,733 mg Trolox Equivalent/100 g dry weight for FRAP. The experimental checking of results revealed the validity of elaborated models and their suitability for the prediction of both responses. The developed mathematical models have expressed a high level of significance through RSM optimisation processes for phenolic antioxidants of propolis.

Lactoferrin Reduces Surfactant Content in the Self-Emulsifying Drug Delivery System.

Self-emulsifying drug delivery systems (SEDDSs) can effectively be employed to formulate drugs with poor oral bioavailability due to low aqueous solubility and high first-pass metabolism. High surfactant content is an existing challenge toward the successful application of SEDDS. A SEDDS is developed with lactoferrin, a natural emulsifier to reduce the Tween content of a fenofibrate (FEN) formulation. FEN SEDDS (SEDDS without lactoferrin) and FEN Lf-SEDDS (SEDDS with lactoferrin) were developed with 30% and 21% Tween content, respectively. Both formulations containing Crodamol GTCC as a lipid component were thermodynamically stable. No significant difference was observed in zeta potential (-9.25 to -12.63 mV), drug content (>85%), and percentage transmittance (>99%) between the two formulations. FEN Lf-SEDDS resulted in higher viscosity and larger particle size than FEN SEDDS. Solidified SEDDS with Aerosil 200 significantly improved in vitro drug release from both formulations than pure FEN. However, FEN SEDDS and FEN Lf-SEDDS did not show a significant difference in cumulative percent release or dissolution efficiency at 120 min. It can be concluded that lactoferrin containing SEDDS with 27% lesser synthetic surfactants (Tween 80 and Span 80) can result in similar physicochemical characteristics. Oral pharmacokinetic study of FEN Lf-SEDDS in a rat model resulted in 1.3 and 5.5 times higher relative bioavailability than marketed product and pure drug, respectively. The addition of lactoferrin could substitute synthetic surfactants in self-emulsifying drug delivery systems significantly.

DESIGN AND IN VIVO EVALUATION OF NAPROXEN-LOADED TRANSFEROSOMAL GEL FOR TRANSDERMAL DELIVERY

Objective: The main objective of the present study was to formulate, optimize, and evaluate naproxen transfersomal gels. Methods: Reverse phase evaporation was used to create thirteen different formulations of naproxen-loaded transfersomes. Using Response Surface Methodology (RSM) and Central Composite Designs (CCD), the influence of independent process variables, such as soy lecithin, cholesterol content and surfactant concentration, on dependent variables, such as entrapment effectiveness and vesicle size of naproxen transfersomes, was assessed. In vitro, ex-vivo, and in vivo drug release of formulations were also studied. Results: It was discovered that the NTG7 formulation of transfersomes had the maximum entrapment effectiveness and ideal vesicle diameter. The optimized NTG7 formulation displayed a maximum drug content of 97.4% and a maximum drug release of 88.03%. The release of naproxen from the final gel adhered to the Korsmeyer-Peppas release model. The ex-vivo drug release of the optimized formulation was found to be 85.91% for 24 h. The maximum drug concentration after oral administration was 843.54±7.67ng/ml, and Tmax was 3.0±0.08h. The improved formulation's AUC0-∞ was greater than the commercial formulation's. A higher drug concentration in the blood compared to the marketed formulation suggested better systemic absorption of naproxen from the gel formulation. After three months, at a temperature range of 2 to 8 °C, the formulation demonstrated correct semisolid consistency and good stability and there was also no appreciable change in the initial values of appearance, pH, and % drug content. Conclusion: The above findings imply that the gel created using naproxen-loaded transfersomes may be a potentially valuable new formulation.

Exploring the effects of diverse extraction methods on nanoemulsion formulation using betel leaf essential oil: Assessing antibacterial efficacy against pathogenic microorganisms

The present study focused on observing the impact of different pretreatments applied on betel leaves powder (BLP) before extraction of essential oil (EO) on the formulation and characterization of BLP-EO-nanoemulsion (NE). BLP-EO nanoemulsion was produced from different BLP-EO (C, CP, MW, CPAMW treated BLP-EO), surfactant (tween 80), and distilled water by ultrasonic probe method and their particle size, polydispersity index (PDI), zeta potential, turbidity, viscosity, refractive index, whiteness index and antibacterial properties were investigated. Significant differences were observed among the nanoemulsions prepared from EO obtained using different pretreatment. The CPAMW-BLP-EO- nanoemulsion prepared with 1% oil concentration and 1:3 oil to surfactant concentration showed the smallest particle size (98.00 ± 0.92 nm), lowest PDI value (0.21 ± 0.01) and zeta potential value (−24.73 ± 1.37) followed by MW, CP and C-BLP-EO-NE due to high concentration of chemical composition that effectively bind with a surfactant. Similarly, better physical properties were obtained for CPAMW-BLP-EO-NE. This CPAMW treated BLP-EO nanoemulsion was the most effective against Gram-positive bacteria like Staphylococcus aureus with an inhibition zone of 12.5 mm than Gram-negative bacteria like Salmonella spp and Escherichia coli with an inhibition zone of 9.4 mm, and 8.5 mm respectively followed by MW, CP, and C treated BLP-EO-NE. In conclusion, the potent antibacterial activity of the nanoemulsion is due to its higher concentration of oxygenated terpenoids and smaller particle size, facilitating effective transport of active compounds and enhancing interactions with microbial cell membranes. Therefore, the CPAMW pre-treated BLP-EO nanoemulsions showed great potential to be incorporated into water-based food products and beverages as flavoring and antimicrobial agents.

Adsorption mechanism of asphaltenes and surfactants at oil-water interface: based on dissipative particle dynamics method

The study of emulsion stabilization mechanisms is of great importance in the field of crude oil extraction, transportation and processing. In order to further investigate the roles of asphaltenes and surfactants in the emulsion stabilization process, the adsorption mechanisms of asphaltenes and surfactants at the oil-water interface were investigated using dissipative particle dynamics. The results show that: the asphaltene interfacial film gradually becomes thicker before the saturation adsorption of asphaltene molecules at the oil-water interface, and the interfacial tension decreases with the increase of the number of molecules until it reaches the equilibrium state; different surfactant molecules have different influences on the interface, and the calculations of the radial distribution function and the interfacial tension show that H2T4 molecules have a stronger effect than H4T4 at the oil-water interface and have stronger surface activity. H2T4 reaches saturation adsorption capacity faster than H4T4 and has higher interfacial efficiency. The asphaltene-surfactant composite system can stabilize the oil-water interface more effectively. Competitive and synergistic effects of asphaltene and surfactant in the process of interfacial adsorption. When the concentration of surfactant in the composite system is low, there is a synergistic effect between the two in the interfacial adsorption process; when the concentration of surfactant is high, there is a competitive effect between the two in the synergistic adsorption process. The surfactant H4T4 has both interfacial adsorption and self-aggregation in the competitive adsorption process. This paper provides ideas for exploring the kinematic laws of molecular behavior in the stabilization mechanism of crude oil emulsions.

Conductometric and spectral analyses of dye-surfactant interactions between indigo carmine and N-alkyltrimethylammonium chloride

The electrical conductivity technique was used to investigate the critical micelle concentration (CMC) of cationic surfactants N-alkyltrimethylammonium chloride (CnTAC; n = 12, 14, 16, and 18). Meanwhile, the interaction between CnTAC and indigo carmine (IC, an anionic dye) was studied using spectrophotometry. Employing the Benesi-Hildebrand and Scott equations, the binding constant (Kb) of IC to the cationic micelles was determined. Calculation of the Gibbs free energy (ΔG) revealed the tendency of IC to bind to micelles. The association between IC and CnTAC clearly depends on the CnTAC concentration: a lower surfactant concentration disrupts the IC-CnTAC complex and decreases IC adsorption, while a higher surfactant concentration has the opposite effect. The alkyl chain length of CnTAC was also found to affect the CMC, Kb, and thermodynamic parameters. A longer alkyl chain reduces the CMC and ΔG and increases Kb, leading to increased solubilization and high spontaneity of the dye. The binding of IC to micelles is ranked as C12TAC < C14TAC < C16TAC < C18TAC.

Surfactant-assisted synthesis of plate-like CuS particles for high-performance symmetric capacitor

In this research, plate-like CuS particles were synthesized through a hydrothermal method using cetyltrimethylammonium bromide (CTAB) and polyvinylpyrrolidone (PVP) as surfactants. The effects of surfactant type and content on the structural, microstructural, and electrochemical properties were explored by the various characterization techniques. Single-phase CuS powders with a space group of P63/mmc were crystallized by decomposition of the copper-thioacetamide complex during hydrothermal treatment. The spherical morphology transformed into plate-like particles by adding the CTAB surfactant, while the PVP surfactant led to an agglomeration of small spherical nanoparticles. With adding the CTAB surfactant, the specific capacitance increased from 630 to 1806 Fg−1 at a current density of 1 Ag−1, while it increased up to 1575 Fg−1 for the PVP surfactant. A symmetric capacitor was assembled on the base of spherical CuS nanoparticles as the negative electrode and the platelike CuS particles as the positive electrode. The CuS//CuS capacitor exhibited comparable electrochemical performance including an energy density of 25.62 Whkg−1 and a power density of 1488 Wkg−1, respectively.

Factors Affecting Stability of Particle Size in Tocotrienol Emulsion Prepared by Spontaneous Emulsification

Incorporation of vitamins into food, feed, and personal care is realised through microencapsulation of their nanoparticle in powder form. Vitamin E consisting of α-, β-, γ-, and δ-tocopherols and α-, β-, γ-, and δ-tocotrienols, is a powerful antioxidant that has been used in food applications and supplements. However, due to its fat-soluble characteristic, the application of tocotrienol in food and beverages is still limited. Therefore, microencapsulation of tocotrienol via emulsification could help maximise the dissolution of tocotrienols during processing and prolong the product’s shelf lives. In this study, factors affecting the particle size, including surfactant concentration, stirring time and speed, and mixing temperature for the preparation of tocotrienol emulsion, were investigated. Emulsions were prepared using 12 wt% surfactant concentration, 800 rpm stirring for 30 minutes. Emulsions with 190 nm particle size were found stable after 30 days storage at ambient temperature.

A two-field formulation for surfactant transport within the algebraic volume of fluid method

Surfactant transport plays an important role in many technical processes and industrial applications such as chemical reactors, microfluidics, printing and coating technology. High fidelity numerical simulations of two-phase flow phenomena reveal rich insights into the flow dynamics, heat, mass and species transport. In the present study, a two-field formulation for surfactant transport within the algebraic volume of fluid method is presented. The slight diffuse nature of representing the interface in the algebraic volume of fluid method is utilized to track the concentration of surfactant at the interface as a volumetric concentration. Transport of insoluble and soluble surfactants is investigated by tracking two different concentrations of the surfactant, one within the bulk of the liquid and the other one at the interface. These two transport equations are in turn coupled by source terms considering the ad-/desorption processes at a liquid–gas interface. Appropriate boundary conditions at a solid–fluid interface are formulated to ensure surfactant conservation, while also enabling to study the ad-/desorption processes at a solid–fluid interface. The developed numerical method is verified by comparing the numerical simulations with well-known analytical and numerical reference solutions and applied to a surfactant-laden drop in shear flow. The presented numerical methodology offers a seamless integration of surfactant transport into the algebraic volume of fluid method, where the latter has many advantages such as volume conservation and an inherent ability of handling large interface deformations and topological changes.

Systematic Investigation on the Surfactant‐Assisted Liquid‐Phase Exfoliation of MoS2 and WS2 in Water for Sustainable 2D Material Inks

MoS2 and WS2 have gathered significant attention due to their tunable properties and wide range of applications. Liquid‐phase exfoliation (LPE) is a facile method to prepare 2D MoS2 and WS2. Currently, the principally employed solvents for LPE of MoS2 and WS2 are expensive and toxic, and have high boiling points. These drawbacks encourage to find more sustainable alternatives to the liquid medium used for the preparation of 2D material inks. Water is the best option, but surfactants are necessary for LPE in water, since MoS2 and WS2 are hydrophobic. Organic molecules with amphoteric character such as sodium dodecyl sulfate, sodium dodecylbenzene sulfonate, and sodium hexadecyl sulfonate (SHS) are selected as suitable candidates for the role. However, the study of these surfactants used in LPE is barely systematically reported. In this work, a detailed investigation is presented on their impact on the LPE of MoS2 and WS2, which are representatives of transition‐metal dichalcogenides. By characterizing and qualifying the products from average number of layers, it is found that all the surfactants work efficiently to exfoliate MoS2 and WS2 into few layers, and SHS stabilizes the 2D layers better than the other two. However, in terms of yield and relative surfactant concentration, a real trade‐off is not identified between maximized quantity of exfoliated materials and minimized surfactant concentration, which prompts to select the colloidal ink based on the specific further needs for processing.

Surface coverage ratio of contaminated Taylor bubbles in a square microchannel

Experiments on contaminated Taylor flows in a microchannel were carried out to investigate the surface coverage ratio for different surfactant properties. Nitrogen and water were used for the gas and liquid phases, respectively. Triton X-100, sodium dodecyl sulfate (SDS) of 90% purity and SDS of 99% purity were used as surfactant. The cross section of the microchannel was square and its width was 200μm. The gas and liquid volumetric fluxes were 0.54 and 0.50 m/s, respectively. Taylor flows were formed by mixing the two phases at the T-junction. Shapes of Taylor bubbles were observed using a microscope and a high-speed video camera. The liquid film thickness changed in the film region, demonstrating that a steep gradient of the interfacial surfactant concentration was formed there. The interface was therefore separated into the clean interface region and the immobilized region by detecting the change in the liquid film thickness. The surface coverage ratio estimated from bubble shapes agreed with that measured from the reduction in the bulk concentration due to surfactant separation by bubbles. The surface coverage ratio increased with increasing the bulk concentration and the increasing rate was smaller than that for the adsorption–desorption equilibrium because of the presence of interfacial advection. The data, however, could be fitted by modifying the functional form for the ad-desorption equilibrium. The bulk concentration normalized by the concentration for the breakdown of the logarithmic relation between the surface tension and the concentration given by the isotherm worked for correlating the surface coverage ratio for the three different surfactants, which can be understood from the order of magnitude of the Marangoni stress.

Experimental study on heat transfer performance enhancement of pulsating heat pipes induced by surfactants

Pulsating heat pipe (PHP) is considered as a promising technique to address the thermal dissipation issues in micro-electronic devices, but its heat transfer performance needs to be further enhanced urgently. In this study, the PHP comprehensive performance experimental system was established. Then, the influence of surfactant sodium dodecyl sulfate (SDS) aqueous solution on the heat transfer performance of PHP was experimentally investigated and the visualization of PHP with surfactant was also accomplished. Additionally, based on Marangoni effect and surface tension, a comprehensive analysis was conducted on the impact mechanism of surfactants on PHP. The experimental results indicated that the oscillatory disturbance of the liquid slug inside the PHP is enhanced by the addition of SDS, and the resulting pressure imbalance and temperature difference enhance the directional flow of the working fluid. Meanwhile, under the operating conditions of 30 W working thermal power and the solution concentration of 0.001 wt%, the thermal resistance of PHP was reduced by 30.7 % compared with that of deionized water (DI water). This indicated that the working fluid with low concentration SDS could increase the area of liquid film and reduce the thermal resistance, which is induced by the surface tension and Marangoni effect due to the uneven distribution of surfactants. However, the thermal resistance of PHP with the SDS concentration of 0.2 wt% is higher than that of DI. This means that high concentration of SDS would deteriorate the startup characteristics and the heat transfer performance of PHP. Therefore, high concentrations of surfactants should be avoided from practical application of PHP.

Investigation of synergistic mechanism of magnesium ions and cationic surfactant in low-rank coal flotation

The effect of magnesium ions on the adsorption of DTAB (Dodecyltrimethylammonium Bromide) surfactants by low-rank coal using adsorption experiments and microscopic mechanism analysis. In addition, the flotation recovery of coal was summarized for application by micro flotation test. The results of adsorption experiments showed that 0.1 mM magnesium ions concentration is optimal, with 12.55 mg/g adsorption capacity. Besides, correlation analysis reveals that the adsorption capacity is positively correlated with temperature, surfactant concentration, reaction time and the magnesium ions density. Adsorption thermodynamics and kinetics experiments indicate that magnesium ions promote adsorption by increasing the adsorption active sites of coal and accelerating the adsorption rate of DTAB on coal. Furthermore, the results of contact angle, zeta potential, model calculations and FTIR (Fourier transform infrared spectroscopy) analyses reveal that magnesium ions and its hydrolysates can adsorb on the coal as a bridge and destroy the stable hydrogen bond on the coal to activate the adsorption, which enhance the negatively charged coal to electrostatically adsorb positively charged DTAB. Moreover, the recovery rate of low-rank coal flotation using DTAB combined with magnesium ions was tested by a micro flotation apparatus, which provides a guidance for the flotation application by saline surfactant solution on coal.

Removal of furosemide from water by emulsion liquid membrane: Influence of experimental conditions and real water matrices

This work investigates the removal of furosemide (FSM) from low pH aqueous phase by emulsion liquid membrane (ELM). The influence of various experimental conditions on FSM permeation rate and subsequent emulsion stability, such as surfactant concentration, diluent type, stripping solution concentration, feed solution pH, stripping solution/membrane solution volume ratio, emulsification time and speed, stirring rate, initial FSM concentration, and emulsion/feed solution volume ratio, was evaluated. The ability to extract FSM in different natural complex matrices was examined. The ELM system is formed by Span 80 (5% w/w) as surfactant, hexane as diluent, NaOH (0.01 N) as stripping agent, stripping solution/membrane solution volume ratio of 1/1, treatment volume ratio of 20/200, and mixing rate of 200 rpm. The treatment process demonstrates complete removal of FSM within a remarkably short time span of 20 min. In seawater and natural mineral water, the extraction efficiency is 94.3% and 96.8%, respectively, after 20 min. Additionally, the stripping efficiency of FSM is reported to be excellent (100%), demonstrating the remarkable ability of ELM to remove and recover FSM from water. For these reasons, the ELM technique is a particularly interesting process for treating FSM-contaminated water.