Salt Surfactant Research Articles

Nanoscopic wetting behaviour of single oil droplets on a fibre

Multiphase fluids that contain dispersed oil droplets are fundamental to many industrial processes and formulated products. In the present work, the surface wetting and interaction between an emulsion droplet and a single fibre were quantitatively investigated as a function of surfactant chemistry, pH, and salt concentration using an optical tweezers apparatus. Silicone droplets were emulsified in water and stabilised by surfactants. An individual droplet was captured using an optical tweezers setup to allow a controlled contact with a fibre surface. During the approach process, the surface interaction was measured and spreading behaviour was quantified after contact was made between the droplet and fibre. Salt concentration was increased to change the surface interaction behaviour. The pH and ζ-potential of silicone emulsions decreased from 9.5 to 6.0 and from 39 mV to − 15 mV, respectively, when increasing salt concentration for both of the surfactants studied, SDS and CTAB. The attraction between the fibre and a silicone oil droplet was found to increase as the electrostatic repulsion was suppressed with an increased salt concentration. This was confirmed by an increased number of droplet-fibre adhesion events and in some cases droplet spreading on the fibre. Such observations for adhesion are based on electrostatic attractions exceeding the maximum force that can be exerted by the trapping laser. When adhesion was not observed, attraction could still be recorded through a thin-film hydrodynamic suction effect during the process of retraction, which becomes more pronounced on the polyester fibre. Our results provide a novel method to directly quantify the surface interaction and wetting of liquid droplets on microscopic fibres simultaneously, which could be valuable when investigating formulated products that involve emulsion droplets.

A novel approach for sludge deep-dewatering via flowing-out enhancement but not relying on cell lysis and bound water release

Effective deep-dewatering is crucial for wastewater sludge management. Currently, the dominant methods focus on promoting cell lysis to release intracellular water, but these techniques often lead to secondary pollution and require stringent conditions, limiting their practical use. This study explores an innovative method using a commercially available complex quaternary ammonium salt surfactant, known as G-agent. This agent remarkably reduces the sludge water content from 98.6 % to 56.8 % with a low dosage (50 mg/g DS) and under neutral pH conditions. This approach surpasses Fenton oxidation in terms of dewatering efficiency and avoids the necessity for cell lysis and bound water release, thereby reducing the risk of secondary pollution in the filtrate, including heavy metals, nitrogen, phosphorus, and other contaminants. The G-agent plays a significant role in destabilizing flocs and enhancing flocculation during the conditioning and initial dewatering stages, effectively reducing the solid-liquid interfacial affinity of the sludge. In the compression filtration stage, the agent's solidification effect is crucial in forming a robust skeleton that improves pore connectivity within the filter cake, leading to increased water permeability, drainage performance and water flow-out efficiency. This facilitates deep dewatering of sludge without cell lysis. The study reveals that the G-agent primarily improves water flow-out efficiency rather than water flowability, indicating that cell lysis and bound water release are not indispensable prerequisites for sludge deep-dewatering. Furthermore, it presents an encouraging prospect for overcoming the limitations associated with conventional sludge deep-dewatering processes.

Investigation on foam properties of Gemini quaternary ammonium salt containing hydroxyl hydrophilic headgroup

Four Gemini quaternary ammonium salts, tetramethylene-1,4- bis [N, N-bis(hydroxypropyl)-hexa/decyloxypropylammonium] bromide (GC6/10-P) and tetramethylene-1,4-bis [N, N-bis(hydroxyethyl)-hexa/decyloxypropylammonium] bromide (GC6/10-E) were synthesized by two-step reactions. This study analyzes the foam properties, including foamability, foam stability, and foam size distribution, of GC6/10-P and GC6/10-E using the Foamscan method. The influence of surfactant concentration and gas flow rate on the properties of Gemini quaternary ammonium salt foam was also studied. Additionally, the relationship between surfactant structure and foam morphology in aqueous solutions was discussed. The results show that all four types of Gemini quaternary ammonium salt surfactants are low-foaming surfactants. The foam capacity (FC) sequence is as follows: GC10-E > GC10-P > GC6-E > GC6-P. The foamability and foam stability are enhanced with increasing surfactant concentration, which increases the adsorbed quantity of surfactant molecules at the air-water interface. The foam produced by GC6-P/E systems is the most unstable; the foam behaviors show faster Ostwald ripening and drainage process in aqueous system. It seems that 150–200 mL/min is an ideal air intake speed. The presence of hydroxyl in the molecular structure enhances the formation of hydrogen bonding between surfactants and water molecules, leading to greater molecular compactness. The results indicate that the foaming behavior of hydroxyl Gemini quaternary ammonium salts can be correlated with concentration and alkyl chains. Foamscan are proposed to research the foaming and foam stability behavior and provide a useful guide for evaluating the foamability of cationic surfactants-based systems, especially in the development of environmentally friendly foam systems suitable for low-foaming products.

Diamond-Like Carbon: A Surface for Extreme, High-Wear Environments.

In this study, we present an in-depth characterization of a diamond-like carbon (DLC) film, using a range of techniques to understand the structure and chemistry of the film both in the interior and particularly at the DLC/air surface and DLC/liquid interface. The DLC film is found to be a combination of sp2 and sp3 carbon, with significant oxygen present at the surface. The oxygen seems to be present as OH groups, making the DLC somewhat hydrophilic. Quartz-Crystal Microbalance (QCM) isotherms and complementary neutron reflectivity data indicate significant adsorption of a model additive, bis(2-ethylhexyl) sulfosuccinate sodium salt (AOT) surfactant, onto the DLC from water solutions and indicate the adsorbed film is a bilayer. This initial study of the structure and composition of a model surfactant is intended to give a clearer insight into how DLC and additives function as antiwear systems.

Surfactant-Aided Stabilization of Individual Carbon Nanotubes in Water around the Critical Micelle Concentration.

Surfactants are widely used to disperse single-walled carbon nanotubes (SWCNTs) and other nanomaterials for liquid-phase processing and characterization. Traditional techniques, however, demand high surfactant concentrations, often in the range of 1-2 wt/v% of the solution. Here, we show that optimal dispersion efficiency can be attained at substantially lower surfactant concentrations of approximately 0.08 wt/v%, near the critical micelle concentration. This unexpected observation is achieved by introducing "bare" nanotubes into water containing the anionic surfactant sodium deoxycholate (DOC) through a superacid-surfactant exchange process that eliminates the need for ultrasonication. Among the diverse ionic surfactants and charged biopolymers explored, DOC exhibits the highest dispersion efficiency, outperforming sodium cholate, a structurally similar bile salt surfactant containing just one additional oxygen atom compared to DOC. Employing all-atomistic molecular dynamics simulations, we unravel that the greater stabilization by DOC arises from its higher binding affinity to nanotubes and a substantially larger free energy barrier that resists nanotube rebundling. Further, we find that this barrier is nonelectrostatic in nature and does not obey the classical Derjaguin-Landau-Verwey-Overbeek (DLVO) theory of colloidal stability, underscoring the important role of nonelectrostatic dispersion and hydration interactions at the nanoscale, even in the case of ionic surfactants like DOC. These molecular insights advance our understanding of surfactant chemistry at the bare nanotube limit and suggest low-energy, surfactant-efficient solution processing of SWCNTs and potentially other nanomaterials.

Synthesis and Aggregation Behavior of Hexameric Quaternary Ammonium Salt Surfactant Tz-6C12QC.

A hexameric quaternary ammonium salt surfactant Tz-6C12QC featuring a rigid triazine spacer and six ammonium groups was synthesized. The molecular structure and aggregation behavior of Tz-6C12QC were characterized by nuclear magnetic resonance spectroscopy, surface tension, conductivity, dynamic light scattering, and transmission electron microscopy, etc. Dissipative particle dynamics (DPD) simulation was employed to investigate the self-assembly behavior of Tz-6C12QC at different concentrations. The rheological behavior of the polyacrylamide/Tz-6C12QC system was characterized by shear rheology. The results indicated that Tz-6C12QC exhibited superior surface activity and lower surface tension compared to conventional surfactants. Rheology analysis revealed that Tz-6C12QC had a significant viscosity reduction effect on polyacrylamide. DLS and TEM indicated that, as the concentration of Tz-6C12QC increased, monomer associations, spherical aggregations, vesicles, tubular micelles, and bilayer vesicles were sequentially formed in the solution. This study presents a synthetic approach for polysurfactants with a rigid spacer and sheds light on the self-assembly process of micelles.

Influence of dialkyl chains of sulfosuccinate sodium salt surfactant on interfacial tension between hydrophobic material and water

We investigated the interfacial tension between a hydrophobic solid and aqueous solutions of bis(2-ethylhexyl) sulfosuccinate sodium salt (AOT), its analogues with different hydrophobic chains, and sodium dodecyl sulfate (SDS). The hydrophobic solid surface was prepared through chemisorption by n-octadecanthiol on an Au film on glass slide. As the hydrophobic oil, triolein was used. It was shown that sulfosuccinate surfactants largely decreased the interfacial tension between the hydrophobic solid and the aqueous solutions compared to SDS. Furthermore, it was observed that a 20 mM AOT aqueous solution induced spontaneous detachment of a triolein droplet from the hydrophobic solid surface in water. This concentration of AOT solution for the detachment was consistent with that expected through the calculation of the spreading coefficient.

Surface Activity, Wetting, and Aggregation of a Perfluoropolyether Quaternary Ammonium Salt Surfactant with a Hydroxyethyl Group.

This paper reports the synthesis of a novel quaternary surfactant containing a hydroxyethyl group (PFPE-C) and the surface properties of its aqueous solution (investigated by comparisons with two structurally similar chemicals, dodecyl-(2-hydroxyethyl)-dimethylammonium chloride (DHDAC) and PFPE-A). The minimum surface tension (γCMC) and critical micelle concentration (CMC) of the PFPE-C aqueous solution were 17.35 mN/m and 0.024 mmol/L, respectively. This study confirms that surfactants containing hydroxyethyl groups efficiently reduce the surface tension of aqueous solutions, and fluorocarbon surfactants exhibit better surface activity than ordinary hydrocarbon surfactants with similar structures. The micellization, aggregation, air-water interfacial adsorption, and wettability of PFPE-C aqueous solutions have been systematically investigated. Highly concentrated PFPE-C aqueous solutions exhibit good wettability on PTFE and paraffin films. Moreover, the aggregates of PFPE-C in the aqueous solution were clearly seen as vesicles on Cryo-TEM micrographs. Primary biodegradation results indicate that 19% of PFPC-C can be degraded within one week.

Effect of the bile salt surfactant sodium taurodeoxycholate on the physicochemical properties of a mixed system of Galangin-Hemoglobin and Baicalein-Hemoglobin

A surfactant that can regulate interactions between drugs and proteins would be a material that is medicinally excipient and biomimetic that has great theoretical and practical significance. Thus, the interactions and binding mechanism of flavonoid isomers [galangin (Gal) and baicalein (Bai)] and hemoglobin (HB) under physiological conditions were studied using multispectral methods, dynamic light scattering (DLS), and antioxidant, antibacterial, and cytotoxicity assay techniques. Then, one bile salt biosurfactant [sodium taurodeoxycholate (NaTDC)] was added to explore the effects that it has on the interactions and functional properties of Gal-HB and Bai-HB systems. For Gal-HB and Bai-HB systems, the fluorescence quenching mechanism of flavonoids on HB was always a static quenching. Driven mainly by electrostatic forces, the conformation of HB became loose, and its secondary structure changed as a result of the presence of Gal or Bai. Three adjacent hydroxyl groups on the A-ring had an obvious binding interaction with protein, and thus, Bai had a stronger binding affinity with HB than Gal, and this has a greater influence on the secondary structure of HB than Gal. In the presence of NaTDC, the binding constants were significantly increased for both systems; also, the antioxidant character, stability, solubility, antibacterial properties, and cancer cell growth inhibition of flavonoids were improved to a certain extent. These findings help us understand the pharmacokinetics, pharmacodynamic function and mechanism of Gal and Bai at the molecular level and also lay the scientific foundation for the design of flavonoid-based foods and drugs.

Inducing an LCST in hydrophilic polysaccharides via engineered macromolecular hydrophobicity

Thermoresponsive polysaccharide-based materials with tunable transition temperatures regulating phase-separated microdomains offer substantial opportunities in tissue engineering and biomedical applications. To develop novel synthetic thermoresponsive polysaccharides, we employed versatile chemical routes to attach hydrophobic adducts to the backbone of hydrophilic dextran and gradually increased the hydrophobicity of the dextran chains to engineer phase separation. Conjugating methacrylate moieties to the dextran backbone yielded a continuous increase in macromolecular hydrophobicity that induced a reversible phase transition whose lower critical solution temperature can be modulated via variations in polysaccharide concentration, molecular weight, degree of methacrylation, ionic strength, surfactant, urea and Hofmeister salts. The phase separation is driven by increased hydrophobic interactions of methacrylate residues, where the addition of surfactant and urea disassociates hydrophobic interactions and eliminates phase transition. Morphological characterization of phase-separated dextran solutions via scanning electron and flow imaging microscopy revealed the formation of microdomains upon phase transition. These novel thermoresponsive dextrans exhibited promising cytocompatibility in cell culture where the phase transition exerted negligible effects on the attachment, spreading and proliferation of human dermal fibroblasts. Leveraging the conjugated methacrylate groups, we employed photo-initiated radical polymerization to generate phase-separated hydrogels with distinct microdomains. Our bottom-up approach to engineering macromolecular hydrophobicity of conventional hydrophilic, non-phase separating dextrans to induce robust phase transition and generate thermoresponsive phase-separated biomaterials will find applications in mechanobiology, tissue repair and regenerative medicine.

Organophilic clays for efficient removal of eosin Y dye properties

organophilic local clay materials from Boyolali- Central of Java were prepared via exchange reaction with hexadecyltrimethylammonium bromide (C16TMABr) solution. These materials were used as potential agent for the removal of an acidic eosin Y dye from artificially polluted solution. Different techniques were used to characterise these materials. The uptake amount of surfactants depended on the initial surfactant loadings, different increase of interlayer spacing of clay layers were obtained due to different orientations of the intercalated surfactants. TGA and DSC data indicated that the intercalated surfactants behave differently than the pure surfactant salt, and it was supported by FTIR studies The eosin removal was operated under various conditions such as dye initial concentrations, different amounts of surfactants, solid dose, temperature, and pH. The pH of removal could be attained by modifying the eosin Y solution or the treatment of the organophilic solid by different acid or basic solutions prior adding to natural eosin Y solution. Good removal efficiencies were obtained at acidic pH below 4.The studied materials exhibited a maximum removal capacity of 78.05 mmol/kg, depending of up take amount of C16TMA cations. The removal trials were found to be endothermic and spontaneous. The reactivity of the different dye forms at different pHs values towards the organophilic clay was compared based on the highest occupied molecular orbital (HOMO) and lowest unoccupied molecular orbital (LUMO) energy values. The regeneration process of spent organophylic clays by a friendly method to the environment was reported and tested over seven successive cycles. Single stage adsorber design was proposed using Langmuir and balance equations, for various volumes of dye solutions at fixed initial concentration and different reduction percentages.

Efficiency and microbial community characteristics of strong alkali ASP flooding produced water treated by composite biofilm system.

Strong alkali alkali-surfactant-polymer (ASP) flooding produced water is a by-product of oil recovery, and it is a stable system composed of petroleum, polyacrylamide, surfactant, and inorganic salts. Efficient, green, and safe ASP produced water treatment technology is essential for oilfield exploitation and environmental protection. In this study, an anaerobic/anoxic/moving bed biofilm reactor with a microfiltration membrane was established and assessed for the real strong alkali ASP flooding produced water (pH 10.1-10.4) treatment. The results show that the average removal rates of COD, petroleum, suspended solids, polymers and surfactants in this process are 57, 99, 66, 40, and 44%, respectively. GC-MS results show that most of the organic compounds such as alkanes and olefins in the strong alkali ASP produced water are degraded. Microfiltration membrane can significantly improve the efficiency and stability of sewage treatment system. Paracoccus (AN), Synergistaceae (ANO) and Trichococcus (MBBR) are the main microorganisms involved in the degradation of pollutants. This study reveals the potential and adaptability of composite biofilm system in treating the produced water of strong alkali ASP produced water.

Preparation of degradable amphoteric surfactant and property evaluation of clean fracturing fluid

AbstractThe main agent of clean fracturing fluid, cationic quaternary ammonium salt surfactant, is difficult to degrade in natural conditions because of its long alkyl chain. In this study, a biodegradable amphoteric surfactant, stearate sulfobetaine (SESB), was synthesized by esterification of long‐chain stearic acid and N,N‐dimethyl ethanolamine followed by quaternization to serve as the main agent of clean fracturing fluid. The structure of the synthetic degradable surfactant was verified by infrared and 1H‐nuclear magnetic resonance spectroscopies. In addition, a series of indoor performance evaluations were carried out, including shear resistance, viscoelasticity, sand carrying capacity, and gel‐breaking performance. A series of experimental evaluations showed that the clean fracturing fluid prepared with 2% SESB and 0.4% EDTA‐4Na had an excellent comprehensive performance. The apparent viscosity was higher than 50 mPa s at 80°C for a shear rate of 170 s−1. It has good heat and shear resistance performance. In addition, the system processed high shear stability and recovery at room temperature. According to the viscoelastic test, the system mainly relies on elasticity to carry sand. The static settling velocity of sand was 0.042 mm/s under high‐temperature conditions of 95°C.

Synthesis and dilute aqueous solution properties of cationic antistatic surfactant functionalized with hydroxyl and ether groups

Abstract Polyester fibers tend to generate and accumulate electrical charges under friction and induction. This significantly affects the production and use process and even poses the risk of electric shocks and fire. Quaternary ammonium salt surfactants with a positive charge can be adsorbed on negatively charged polyester fibers and have excellent antistatic properties. Therefore, we have synthesised a cationic antistatic surfactant functionalised with hydroxyl and ether groups: N-hexadecyl-N,N-dimethyl-N-butanoxy glycerol ether ammonium chloride (HDBGA). The structure was characterized by 1H NMR, FTIR and ESI/MS. The excellent properties of HDBGA in aqueous solution were investigated by measuring the Krafft point (TK), surface tension, conductivity, and steady-state fluorescence. Also antistatic tests were carried out. The results show that the TK of HDBGA is below 0 °C indicating that it can still be applied in cold water. The new quaternary ammonium compound could effectively decrease the surface tension of aqueous solution to 31.28 mN m−1, where the critical micelle concentration (CMC) at 298.15 K was 3.83 × 10−4 mol L−1. In addition, the static electricity and static half-life values of the polyester cloths treated with the HDBGA solutions were also measured, as well as the effects on the fabric properties. The product exhibited excellent antistatic properties and satisfactory wash resistance, and the fabric fibers were not damaged.

Interfacial properties of cationic and anionic Gemini surfactant mixtures

AbstractThe possibility and the prospect of cationic/anionic (“catanionic”) surfactant mixtures based on sulfonate Gemini surfactant (SGS) and bisquaternary ammonium salt (BQAS) in the field of enhanced oil recovery was investigated. The critical micelle concentration (CMC) of SGS/BQAS surfactant mixtures was 5.0 × 10−6 mol/L, 1–2 orders of magnitude lower than neat BQAS or SGS. A solution of either neat SGS or BQAS, could not reach an ultra‐low interfacial tension (IFT); but 1:1 mol/mol mixtures of SGS/BQAS reduced the IFT to 1.0 × 10−3 mN/m at 100 mg/L. For the studied surfactant concentrations, all mixtures exhibited the lowest IFT when the molar fraction of SGS among the surfactant equaled 0.5, indicating optimal conditions for interfacial activity. The IFT between the 1:1 mol/mol SGS/BQAS mixtures and crude oil decreased and then increased with the NaCl and CaCl2 concentrations. When the total surfactant concentration was above 50 mg/L, the IFT of SGS/BQAS mixtures was below 0.01 mN/m at the studied NaCl concentrations. Adding inorganic salt reduced the charges of hydrophilic head groups, thereby making the interfacial arrangement more compact. At the NaCl concentration was above 40,000 mg/L, surfactant molecules moved from the liquid–liquid interface to the oil phase, thus resulting in low interfacial activity. In addition, inorganic salts decreased the attractive interactions of the SGS/BQAS micelles that form in water, decreasing the apparent hydrodynamic radius (DH, app) of surfactant aggregates. When the total concentration of surfactants was above 50 mg/L, the IFT between the SGS/BQAS mixtures and crude oil decreased first and then increased with time. At different surfactant concentrations, the IFT of the SGS/BQAS mixtures attained the lowest values at different times. A high surfactant concentration helped surfactant molecules diffuse from the water phase to the interfacial layer, rapidly reducing the IFT. In conclusion, the cationic‐anionic Gemini surfactant mixtures exhibit superior interfacial activity, which may promote the application of Gemini surfactant.

Development of Ciprofloxacin-Loaded Bilosomes In-Situ Gel for Ocular Delivery: Optimization, In-Vitro Characterization, Ex-Vivo Permeation, and Antimicrobial Study.

Conventional eye drops are most commonly employed topically in the eye for the management of bacterial conjunctivitis. Eye drops have a low corneal residence time and 90-95% of the administered dose is eliminated from the eye by blinking and the nasolacrimal drainage system. This problem can be minimized by formulating a mucoadhesive ocular in-situ gel system that undergoes sol-gel transition upon stimulation by temperature, pH, and ions. The goal of this study was to develop ciprofloxacin (CIP) loaded bilosomes (BLO) in-situ gel for the improvement of therapeutic efficacy. The BLO was prepared by the thin-film hydration method and optimized by the Box-Behnken design. Cholesterol (CHO), surfactant (Span 60), and bile salt (sodium deoxycholate/SDC) were used as formulation factors. The vesicle size (nm) and entrapment efficiency (%) were selected as responses (dependent factors). The optimized CIP-BLO (CIP-BLO-opt) formulation displayed a vesicle size of 182.4 ± 9.2 nm, a polydispersity index of 0.274, a zeta potential of -34,461.51 mV, and an entrapment efficiency of 90.14 ± 1.24%. Both x-ray diffraction and differential scanning calorimetry spectra did not exhibit extensive peaks of CIP in CIP-BLO-opt, revealing that CIP is encapsulated in the BLO matrix. The CIP-BLO-opt formulation was successfully incorporated into an in-situ gel system using a gelling agent, i.e., Carbopol 934P and hydroxyl propyl methyl cellulose (HPMC K100 M). CIP-BLO-opt in-situ gel formulation (CIP-BLO-opt-IG3) was evaluated for gelling capacity, clarity, pH, viscosity, in-vitro CIP release, bio-adhesive, ex-vivo permeation, toxicity, and antimicrobial study. The CIP-BLO-opt-IG3 exhibited satisfactory gelling properties with a viscosity of 145.85 ± 9.48 cP in the gelling state. CIP-BLO-opt-IG3 displayed sustained CIP release (83.87 ± 5.24%) with Korsmeyer-Peppas kinetic as a best-fitted model (R2 = 0.9667). CIP-BLO-opt-IG3 exhibited a 1.16-fold than CIP-IG and a 2.08-fold higher permeability than pure CIP. CIP-BLO-opt-IG3 displayed a significantly greater bio-adhesion property (924.52 ± 12.37 dyne/cm2) than tear film. Further, CIP-BLO-opt-IG3 does not display any toxicity as confirmed by corneal hydration (76.15%), histology, and the HET-CAM test (zero scores). CIP-BLO-opt-IG3 shows significantly higher (p < 0.05) antimicrobial activity against P. aeruginosa and S. aureus than pure CIP. From all these findings, it could be concluded that CIP-BLO-opt-IG3 might be an effective strategy for the increment of corneal residence time and therapeutic activity of CIP.

PdAu Nanosheets for Visible-Light-Driven Suzuki Cross-Coupling Reactions.

Combining a two-dimensional (2D) morphology and plasmonic photocatalysis represents an efficient design for light-driven organic transformations. We report a one-pot synthesis of surfactant templated PdAu nanosheets (NSs). Transmission electron microscopy (TEM) and X-ray photoelectron spectroscopy (XPS) analyses show the formation of 2D PdAu structures was initiated through nanoparticle seeds dispersed in the alkyl ammonium salt surfactant which acted as a template for the growth into NSs. The PdAu NSs were used for visible-light-enhanced Suzuki cross coupling. The PdAu bimetallic NSs outperformed monometallic Pd NSs and commercial Pd/C in room-temperature Suzuki cross-coupling reactions. The high catalytic activity is attributed to a combination of the 2D morphology giving rise to plasmon-enhanced catalysis and a high density of surface atoms, the electron-rich Pd surface due to alloying, and the presence of weakly bound amines. A comparative study of surfactant-assisted NSs and CO-assisted NSs was also carried out to assess the influence of surface ligands on the catalytic and photocatalytic enhancement of NSs with similar morphology. The surfactant-assisted NSs showed substantially superior performance compared to the CO-assisted for room-temperature Suzuki coupling reactions.

Study of Surfactant‐Induced Deformations at the Interface of Emulsion Droplets by Digital Image Analysis of Droplet Projections

AbstractEmulsion droplets do not always have smooth surfaces. Under certain conditions, the formation of surface‐active species at oil–water interfaces leads to interfacial instabilities that cause a spontaneous increase in the droplet surface area, which results in fascinating droplet morphologies. The specific system presented in this study consists of stearic acid encapsulated in an oil droplet and the quaternary ammonium surfactant cetyltrimethylammonium bromide in the aqueous phase. This system is studied by examining the deformation of single emulsion droplets hanging on a capillary tip. By using digital image analysis, the relative perimeters and fractal dimensions from the droplet outlines are calculated and the influences of several process parameters on their temporal development are studied. It is demonstrated that the surfactant concentration, pH value, salt addition, alcohol addition, and viscosity have a considerable impact on the droplet morphology and possible causes for this behavior are discussed. Through this study, important insights are gained into the deformation mechanism and kinetics that can potentially guide the future preparation of particles with special surface morphologies.

Antibacterial and biodegradable keratin-based quaternary ammonium salt surfactant potential as hair care additive

Biomass-based surfactants have excellent surface activities, showing the common characteristics of natural biomass including biocompatibility, biodegradability and non-toxicity, which are environmental-friendly and accord with the green development direction. In this study, a keratin based quaternary ammonium salt surfactant (denoted as E-K) was prepared by cationic modification of keratin with epoxypropyldodecyldimethylammonium chloride (EPDDMAC). The characterization of E-K by FTIR and the conversion rate of -NH2 in keratin confirmed the successful preparation of E-K. Subsequently, surface activity such as surface tension (γcmc) and critical micelle concentration (cmc), physicochemical properties such as HLB value, isoelectric point, foaming property and emulsifying property, as well as antibacterial activity and biodegradability were investigated. The results show that E-K possesses good surface activity, acceptable emulsifying and foaming ability. The HLB of E-K is 14-15, and it has excellent compatibility with commercial surfactants commonly used in hair care products. Particularly, E-K is a betaine zwitterionic surfactant, and its isoelectric point increases from 3.8 to 9.2 due to cationization. This means that the quaternized keratin hydrolysate is easily adsorbed on the hair surface, and makes the hair surface smoother and denser, which was proved by the adsorption test and SEM observation. Furthermore, E-K has outstanding antibacterial activity against E. coli and S. aureus, and the BOD5/CODCr value indicated that it is easily biodegradable. Therefore, the prepared biomass-based surfactant (E-K) has great potential application in hair care products and other products related to antibacterial and biodegradable surfactants.

Fabrication of Fe3O4 nanoparticles by using cathode glow discharge electrolysis plasma and its electrochemical properties

In this work, Fe3O4 nanoparticles (NPs) were fabricated by one-step method using cathode glow discharge electrolysis (CGDE) plasma technique in 2.0 g L−1 Na2SO4 solution at 600, 650 and 700 V applied voltage, in which Pt needle point and scrap iron wire were served as cathode and anode, respectively. The fabricated products were characterized by FT-IR, XRD, SEM and TEM. A possible fabrication mechanism of Fe3O4 NPs under CGDE was proposed. In addition, electrochemical performance of Fe3O4 NPs as an electrode material for supercapacitors was investigated by cyclic voltammetry, galvanostatic charge–discharge, and electrochemical impedance spectroscopy in 1 mol L−1 Na2SO3 electrolyte. The results showed that the particle sizes of the fabricated products are below 20 nm, Fe3O4 NPs as the electrode material have good reversibility which can reach 247 F g−1 specific capacitance at current density of 0.5 A g−1, and still keep 41.1% capacity retention after 5000 cycles. Fe3O4 NPs can be regarded as a promising and favorable candidate of electrode materials for supercapacitor. Compared with other methods, CGDE has the advantages of simple experimental equipment, no gas supply, mild reaction conditions and no secondary pollution. It is a green synthesis technique without adding alkali, surfactant and ferric salt containing both Fe2+ and Fe3+.