Surface Tension Measurements Research Articles

Contactless surface tension measurement of molten oxides using oscillating drop method in an aerodynamic levitator

Aerodynamic levitation stands as a contactless method for thermophysical property measurement of molten oxides at high temperatures, offering the advantage of eliminating sample contamination and enabling surface tension measurement through the oscillating drop method. However, the presence of oscillation mode splitting results in an underestimation of surface tension. By improving levitation stability and optimizing the acoustic excitation method for the levitated drops, this study successfully eliminates oscillation mode splitting for the first time. The l = 2 resonance frequency is directly measured, which is used to calculate surface tension according to the Rayleigh equation. Taking Al2O3 as a representative of oxides, this study demonstrates the accurate surface tension measurement during the frequency scan process when oscillation mode splitting is absent. Additionally, combining damped oscillation analysis with the frequency scan reduces measurement uncertainty from 2.8 % to 1.5 %. Within the temperature range of 2336K–2923K, the surface tension of molten Al2O3 is determined to be γ = −(4.071 ± 2.688) × 10−5 (T-2327)+(0.7465 ± 0.074) N/m. Underestimation of surface tension is prevented when the l = 2 resonance frequency is used for surface tension calculations. The frequency crossover method which is used for surface tension measurement is also found to be affected by oscillation mode splitting.

Interfacial property determination from dynamic pendant-drop characterizations.

The properties of the interface between materials have practical implications in various fields, encompassing capillary action, foam and emulsion stability, adhesion properties of materials and mass and heat transfer processes. Studying the dynamics of interfaces is also fundamental for understanding intermolecular interactions, change of molecular conformations and molecular aggregations. Pendant-drop tensiometry and its extension, the oscillating drop method, are simple, versatile methods used to measure surface tension, interfacial tension and interfacial rheological properties. These methods can, however, generate unreliable results because of inadequate material preparation, an incorrect calibration method, inappropriate selection of data for analysis, neglect of optical influences or operating the system outside the linear viscoelastic regime. In addition, many studies fail to report accurate uncertainties. This protocol addresses all these critical points and provides detailed descriptions of some operation tips relating to purifying methods for different kinds of material, the time frame for analyzing measurement data, the correction method for optical effects, implementation of the oscillating method with a common programmable pump and remedies for some common problems encountered during the measurement. Examples of interfacial tension measurements for two- and three-phase systems, as well as interfacial dilational modulus measurements for N2 and surfactant solutions, are provided to illustrate procedural details and results. A single measurement takes minutes to hours to complete, while the entire protocol, including the leak test, cleaning, repeated measurements and data analysis, may take several days.

Surface engineered novel cationic surfactants with enhanced surface adsorption for environmental applications

Gemini Cationic Surfactants (GCS) have garnered significant attention due to their distinctive molecular structure, featuring two hydrophilic head groups associated with a hydrophobic spacer. This distinctive configuration enables diverse applications across various fields. Hence, the current study introduces a novel series of GCSs, ethanediyl-1,2-bis[di(2-hydroxypropyl) alkylammonium] dibromide (Cn-C2-Cn[IsoPr(OH)2; n = 9, 12 and 14) and comprehensively explore their properties, highlighting their promising antimicrobial activity. The synthesis of GCSs was validated using 1H NMR and IR spectroscopy. Dynamic Light Scattering was employed to determine the dimensions of Gemini surfactant aggregates in aqueous solutions. Surface tension analysis determined critical concentrations of micelle (CMC), minimum surface area (Amin) and concentration of surface excess (Γmax). Physicochemical properties were assessed through conductivity and surface tension analyses in aqueous solutions. The CMC, Amin and Γmax values decrease as alkyl chain length extends. Surface tension data revealed strong adsorption of GCSs at interfaces. π values (mN/m) ranged from 36.7 (C14C2C14[Iso-Pr(OH)]2) to 45.3 (C9C2C9[Iso-Pr(OH)]2). Conductivity and surface tension measurements further characterized Gemini surfactants in aqueous environments at 298 K. The size of the micelle aggregates varied between C9C2C9[Iso-Pr(OH)]2 (1.2885 nm) and C14C2C14[Iso-Pr(OH)]2 (1.9210 nm), highlighting the impact of chain length on micelle size. Hence, the study highlights significant effect of the chain lengths on Gemini cationic surfactants’ self-assembly in dilute aqueous environments. Antimicrobial tests demonstrated significant activity of Cn-C2-Cn[IsoPr(OH)]2 GCSs at varying concentrations. Antimicrobial tests showed the significant antimicrobial potential of these GCS compounds, suggesting their potential and promising applications in medical, hygiene, environmental sanitation and advanced materials sectors.

Promoting sustainability: Micellization and surface dynamics of recycled monoethanolamine surfactants

The purpose of this work is to explore the micellization and surface characteristics of recycled monoethanolamine (MEA) surfactants, designated as MK-1, MK-2, and MK-3, and to assess their potential in promoting sustainability. Traditional surfactants contribute to environmental pollution due to their non-renewable sources and persistence in nature. This study addresses the knowledge gap in sustainable surfactant development by investigating the efficacy of recycled MEA surfactants. Its novelty lies in its innovative recycling process, which not only reduces waste, but also produces surfactants with superior properties. This study also investigates the distillation-based separation of MEA from degraded compounds, showcasing its potential in waste management. It was found that a maximum MEA separation of 17 % was achieved with a resulting purity of 83 %. Optimal conditions, including the use of catalysts and a temperature of 393K, led to enhanced oleic acid conversion. Similarly, reactions conducted with catalysts at 433K for 3 h demonstrated favorable outcomes. Surfactant MK-1 exhibited superior foam and emulsifying abilities, generating a foam height of 60 cm with only 8 cm lost after 10 min. Regarding emulsifying properties, the sunflower oil/water system with a 0.1% MK-1 solution exhibited delayed water separation from the emulsion. MK-3 displayed the highest pC20 value at 2.91. Among the MEA-based surfactants, MK-1 reduced surface tension to 33.1 mN/m. The maximum surface excess concentration (Γmax) for all surfactants was consistent. This demonstrates that recycled MEA surfactants exhibited favorable micellization properties, with a critical micelle concentration (CMC) comparable to that of virgin counterparts. Over ten cycles of use and regeneration, the performance of recycled MEA surfactants remained stable. Surface tension measurements indicated improved interfacial activity, while emulsification capacity tests revealed an enhanced performance in forming stable emulsions. This implies the potential of recycled MEA surfactants to produce high-performance surfactants, thereby promoting sustainability in the chemical industry.

High efficacy of chloroquine-derived bile salts in Pluronic F127 micelles against blood-stage Plasmodium falciparum

Colloidal nanocarriers can play a key role in the efficacious delivery of drugs, including antimalarials. Here, we investigated the ability of polymeric micelles of the block copolymer F127 to act as nanovehicles for two organic salts derived from chloroquine and human bile acids, namely, chloroquinium cholate (iCQP1) and chloroquinium glycocholate (iCQP1g). We have previously reported the strong in vitro antiplasmodial activity of these salts, which displayed IC50 values of 13 and 15 nM against blood forms of Plasmodium falciparum, respectively. By deriving from amphiphilic lipids, iCQP1 and iCQP1g also enclose the ability to act as surface-active ionic liquids (SAILs). The micellization properties of neat F127 and of the F127/SAIL mixtures were initially investigated to gain physicochemical insight into the interaction between polymer and bioactive SAILs, resorting to differential scanning calorimetry, surface tension measurements and dynamic light scattering. Micelle formation by F127 is an endothermic process strongly temperature and concentration dependent. Interestingly, this process is significantly changed when the molar fraction of SAIL (xSAIL) in the F127/SAIL mixture is varied between 0.33 and 0.90. Both SAILs favor the formation of mixed micelles by decreasing the micellization temperature, and (observed only when for xSAIL = 0.33) by synergistically decreasing the cmc. Concomitantly, the micellar size is reduced from 18 to 13 nm as xSAIL is increased from 0.33 to 0.90. Crucially, in vitro assays show that when the SAILs are loaded into F127 polymeric micelles, their antiplasmodial efficacy is substantially enhanced, with a significant drop in IC50, especially for the iCQP1/F127 system. This opens new possibilities for the nanoformulations of antimalarial compounds.

Synthesis, Surface Activity, Emulsifiability and Bactericidal Performance of Zwitterionic Tetrameric Surfactants.

In this paper, a series of tetrameric surfactants (4CnSAZs, n = 12, 14, 16) endowed with zwitterionic characteristic were synthesized by a simple and convenient method and their structures were characterized by FT-IR, 1H NMR and elemental analysis. Their physicochemical properties were studied using the Wilhelmy plate method, fluorescence spectra and dynamic light scattering technique. 4CnSAZs have higher surface activities and tend to adsorb at the air/water surface rather than self-assembling in aqueous solution. The thermodynamic parameters obtained from surface tension measurements show that both processes of adsorption and micellization of 4CnSAZs are spontaneous and that the micellization processes of 4CnSAZs are entropy-driven processes. Both adsorption and micellization of 4CnSAZs are inclined to occur with the increase of alkyl chain length or temperature. For 4C12SAZs, there are only small-size aggregates (micelles), while the large aggregates (vesicles) are observed at the alkyl length of 4CnSAZs of 14 or 16. This shows that the alkyl chain length for oligomeric surfactants has a greater sensitivity for aggregate growth. The aggregate morphologies obtained from the calculated values of critical packing parameter (p) for 4C14SAZs and 4C16SAZs can be supported by the DLS measurement results. The test results obtained by the separation-water-time method show that 4CnSAZs have good emulsification performance and that the prepared emulsions appear to exit in the form of multiple emulsions. In addition, 4CnSAZs have good antibacterial activities against Escherichia coli (E. coli) and Staphylococcus aureus (S. aureus). The present study reveals the unique behavior of a zwitterionic tetrameric surfactant and may give new insights into molecular design and synthesis of a high degree of surfactants with different structure characteristics for potential application in various industrial fields.

Characterization of CrMnNi Steel Powders Obtained via Gas Atomization

To obtain a successful product during additive manufacturing, the powder as a raw material must have the high quality. The purpose of this work is to investigate CrMnNi steel powders obtained by inert gas atomization with nickel content: 3, 6, and 9 wt% and to identify dependencies between the powder size and morphology, solidification structure, and change in chemical composition and thermophysical properties. Particle size distribution is measured by a laser scattering analyzer: d50 value are 82.02, 69.32, and 75.54 μm for powders with 3, 6, and 9 wt%, respectively. Surface tension (ST) measurements are made by maximum bubble pressure method: for steels with 3, 6, and 9 wt% at temperature 1500 °C, ST is 1.01, 1.07, and 1.15 mN m−1, respectively. It is found that the change in particle size affects the chemical composition, the content of the ferromagnetic phase and secondary dendritic arm‐spacing. Changes in the content of elements such as S, O, N, and Mn are determined, depending on the diameter of the particles. The influence of changes in content of S, O, and N on the thermophysical properties such as ST is investigated.

Study on the Control of Steam Front Mobility in High-Temperature and High-Salinity Conditions Using Polymer-Enhanced Foam.

This study investigated the enhancing effects of the temperature-resistant polymer Poly(ethylene-co-N-methylbutenoyl carboxylate-co-styrenesulfonate-co-pyrrolidone) (hereinafter referred to as Z364) on the performance of cocamidopropyl hydroxy sulfobetaine (CHSB) foam under high-temperature and high-salinity conditions. The potential of this enhanced foam system for mobility control during heavy oil thermal recovery processes was also evaluated. Through a series of experiments, including foam stability tests, surface tension measurements, rheological assessments, and parallel core flooding experiments, we systematically analyzed the interaction between the Z364 polymer and CHSB surfactant on foam performance. The results indicated that the addition of Z364 significantly improved the strength, thermal resistance, and salt tolerance of CHSB foam. Furthermore, the adsorption of CHSB on the polymer chains enhanced the salt resistance of the polymer itself, particularly demonstrating stronger blocking effects in high-permeability cores. The experimental findings showed that Z364 increased the viscosity of the liquid film, slowed down liquid drainage, and reduced gas diffusion, effectively extending the half-life of CHSB foam and improving its stability under high-temperature conditions. Additionally, in parallel core flooding experiments, the polymer-enhanced foam exhibited significant flow diversion effects in both high-permeability and low-permeability cores, effectively directing more fluid into low-permeability channels and improving fluid distribution in heterogeneous reservoirs. Overall, Z364 polymer-enhanced CHSB foam demonstrated superior mobility control during heavy oil thermal recovery, offering new technical insights for improving the development efficiency of high-temperature, high-salinity reservoirs.

Cardamom Pickering emulsions stabilized by cellulose nanostructures as disinfection agents against bacteria and SARS-CoV-2

This study introduces a new disinfectant agent utilizing cardamom essential oil stabilized by cellulose nanomaterials (CN). The Pickering emulsion technique prevented oil degradation and extended its storage duration. Cellulose nanocrystals (CNC) or cellulose nanofibers (CNF) were utilized as stabilizers, and the emulsions were evaluated for surface tension, rheology, morphology, antimicrobial and antiviral activity against S. enterica, S. aureus, P. aeruginosa, E. coli, and SARS-CoV-2. Surface tension measurements indicated an electrostatic stabilization mechanism in CNC emulsions, exhibiting fluid behavior confirmed by rheological tests. On the other hand, CNF emulsions displayed drop packaging, characteristic of shear-thinning behavior, as confirmed by the Ostwald-de-Waele model. The emulsions exhibited antibacterial activity against S. aureus and P. aeruginosa, particularly the CNC samples, suggesting that nanocellulose alters the regulation of oil migration into the medium. Testing against SARS-CoV-2 revealed that cardamom essential oil required 30 min of contact for viral protein denaturation, while CNC and CNF emulsions took 60 and 50 min, respectively. This indicates that CN acts as an encapsulating agent, prolonging the oil’s release time and necessitating longer contact periods with the virus. These findings demonstrate the potential of these emulsions in developing new antimicrobial and antiviral products.

Effect of oil structure on adsorption behavior of emulsifier at the oil-polyol interface and the emulsion features

The aim of this study was to investigate the effect of oil structure on the dynamic adsorption behavior of emulsifier at the oil-polyol interface and the corresponding emulsion feature. Glycerol was used as the representative polyol, and the emulsifier was Polyglyceryl-2 Dipolyhydroxystearate (PGPH). Three kinds of alkanes and three kinds of ester oils were chosen for investigation. Firstly, the properties of each oil were studied by measuring surface tension (σ), interfacial tension with glycerol (γ0), and affinity between oils and PGPH. The results indicated that there was little difference in the fundamental characteristics of oils, with the exception of GTCC. Due to its triglyceride structure, GTCC exhibited similar polarity to glycerol, resulting in low interfacial tension and a strong affinity with PGPH. Secondly, the interfacial critical micelle concentration (CMCIFT), saturation adsorption amount (Γ∞), Langmuir constant (κ) and minimum molecular area (Amin) of PGPH were obtained by measuring the dynamic interfacial tension of PGPH adsorption at different oil-glycerol interfaces. The experimental results indicate that for alkanes, the longer the alkane chain length and the more the number of branch chains, the higher the emulsifier Γ∞ at the interface, leading to improved emulsion stability. In ester oils, the greater the affinity between the oil and glycerol, resulting in the lower the initial interfacial tension, a smaller Γ∞ and consequently smaller emulsion particle size. However, this also led to poor emulsion stability. Finally, Pearson correlation analysis was conducted between oil properties, adsorption parameters and emulsion size and stability. The results indicated that for alkanes, there was a negative correlation between particle size and emulsion stability with surface tension and Γ∞. In ester oils, there was a strong positive correlation between particle size and interfacial tension as well as κ. Additionally, the creaming of emulsions showed a strong negative correlation with interfacial tension and Γ∞.

Aggression to Biomembranes by Hydrophobic Tail Chains under the Stimulus of Reductant.

Stimulus-responsive materials hold significant promise for antitumor applications due to their variable structures and physical properties. In this paper, a series of peptides with a responsive viologen derivative, Pep-CnV (n = 1, 2, 3) were designed and synthesized. The process and mechanism of the interaction were studied and discussed. An ultraviolet-visible (UV) spectrophotometer and fluorescence spectrophotometer were used to study their redox responsiveness. Additionally, their secondary structures were measured by Circular Dichroism (CD) in the presence or absence of the reductant, Na2SO3. DPPC and DPPG liposomes were prepared to mimic normal and tumor cell membranes. The interaction between Pep-CnV and biomembranes was investigated by the measurements of surface tension and cargo leakage. Results proved Pep-CnV was more likely to interact with the DPPG liposome and destroy its biomembrane under the stimulus of the reductant. And the destruction increased with the length of the hydrophobic tail chain. Pep-CnV showed its potential as an intelligent antitumor agent.

Molecular interactions of the antioxidant in the coolant oil for energy transformers: Dielectric and simulation studies

This research paper presents experimental and theoretical findings concerning the blending of mineral oil and vegetable oils, both with and without antioxidants. The study analyses a variety of parameters for different blends of mineral and vegetable oils, including breakdown voltage, ageing resistance, dielectric constant, viscosity, dissipation factor, surface tension, flash point, and fire point. The study was further extended to investigate the effects of varying the amount of antioxidants added to mineral oil blends with different vegetable oils. The best transformer insulating solution is found by extensive analyses that include measurements of breakdown voltage, flash point, fire point, and surface tension. This blends’ properties with antioxidant are either better than pure mineral oil or comparable to mineral oil. Density functional theory (DFT) analyses the molecular structure and dipole moment of an antioxidant. Molecular dynamics simulation method (MD) analysis of the average water residual time – periods of an antioxidant will show the stability of H-bond interactions. The primary objective of this experiment is to unveil a novel liquid-insulating material that not only excels in dielectric performance but also aligns with environmentally friendly practices.

The Gibbs and Butler Equations and the Surface Activity of Dilute Aqueous Solutions of Strong and Weak Linear Polyelectrolyte-Surfactant Mixtures: The Roles of Surface Composition and Polydispersity.

In a previous paper, we applied a combination of direct measurements of both surface tension and surface excess in conjunction with the Gibbs equation to explain features of the adsorption and surface tension of mixtures of surfactants and strong linear polyelectrolytes at the air-water interface. This paper extends that model by including (i) the restrictions of the Butler equation for the behavior of the surface tension of mixed systems and (ii) the surface behavior of surfactant and linear weak polyelectrolyte mixtures, for which the inclusion of measurements of the surface excess and composition is shown to be particularly important. In addition, a closer examination of earlier data at higher concentrations provides evidence that the surface layering that is often observed in polyelectrolyte-surfactant systems is also an average equilibrium phenomenon and is driven by particular aggregation patterns that occur in some systems and not in others. Although the successful application of the Gibbs and Butler equations indicates that strong polyelectrolyte-surfactant systems can be described in terms of an average equilibrium over wide ranges of concentration, we have identified two concentration ranges where polydispersity in either polyelectrolyte molecular weight or composition results in significant time dependence of the surface behavior.

Dissipative particle dynamics simulation and experimental studies of pseudo-gemini surfactants with different hydrophobic chain lengths

In this work new pseudo-gemini type surfactants are constructed via a simple, energy and material efficient way, using piperazine, propylene oxide and seven different fatty acids: capric, lauric, myristic, stearic, oleic and linolenic. The compounds are characterized by 1H NMR, 13C NMR and FTIR studies. Micellization and adsorption properties of the novel pseudo-gemini surfactants are investigated via surface tension and conductivity measurements. Antimicrobial properties are evaluated using the simple disk diffusion test method. Dissipative Particle Dynamics (DPD) simulations are performed to model aggregation behavior of the new pseudo-gemini surfactants. Experimental studies revealed that Critical Micelle Concentration (CMC) of the obtained pseudo-gemini surfactants are lower than 1 mmol/L. Theoretically calculated CMC values are slightly higher than experimental CMC values. However, overall, very good agreement between theoretical and experimental CMC values is observed. Radial Distribution Function (RDF) and radius of gyration (Rg) plots are analyzed to gain further insight into aggregation of the surfactant molecules in aqueous environment. The DPD model of the pseudo-gemini amphiphiles successfully predicts the most important traits of the aggregation process.

Influence of chirality and sequence in lysine-rich lipopeptide biosurfactants and micellar model colloid systems

Lipopeptides can self-assemble into diverse nanostructures which can be programmed to incorporate peptide sequences to achieve a remarkable range of bioactivities. Here, the influence of peptide sequence and chirality on micelle structure and interactions is investigated in a series of lipopeptides bearing two lysine or D-lysine residues and tyrosine or tryptophan residues, attached to a hexadecyl lipid chain. All molecules self-assemble into micelles above a critical micelle concentration (CMC). Small-angle x-ray scattering (SAXS) is used to probe micelle shape and structure from the form factor and to probe inter-micellar interactions via analysis of structure factor. The CMC is obtained consistently from surface tension and electrical conductivity measurements. We introduce a method to obtain the zeta potential from the SAXS structure factor which is in good agreement with directly measured values. Atomistic molecular dynamics simulations provide insights into molecular packing and conformation within the lipopeptide micelles which constitute model self-assembling colloidal systems and biomaterials.

Stabilization of Fish Protein-Based Adhesive by Reduction of Its Hygroscopicity.

Protein-based fish adhesives have historically been used in various bonding applications; however, due to the protein's high affinity for water absorption, these adhesives become destabilized in high-moisture environments, resulting in reduced bondline strength and early failure. This limitation makes them unsuitable for industrial applications with higher demands. To address this issue, water-insoluble raw powder materials such as iron, copper, or zeolite were incorporated into natural fish adhesives. In this study, the hygroscopicity, dry matter content, thermal analysis (TGA/DSC), FT-IR spectroscopy, surface tension measurements, vapour permeability, and scanning electron microscope (SEM) of the modified adhesives were determined. In addition, the bonding properties of the modified adhesives were evaluated by the tensile shear strength of the lap joints, and mould growth was visually inspected. The resulting modified protein-based adhesives demonstrated improved stability in high humidity environments. Enhancing the hygroscopic properties of protein-based fish adhesives has the potential to unlock new opportunities and applications, providing a healthier and more environmentally sustainable alternative to petroleum-based adhesives.

Quantifying surface tension and viscosity in biomolecular condensates by FRAP-ID

Many proteins with intrinsically disordered regions undergo liquid-liquid phase separation under specific conditions in vitro and in vivo. These complex biopolymers form a metastable phase with distinct mechanical properties defining the timescale of their biological functions. However, determining these properties is nontrivial, even in vitro, and often requires multiple techniques. Here we report the measurement of both viscosity and surface tension of biomolecular condensates via correlative fluorescence microscopy and atomic force microscopy (AFM) in a single experiment (fluorescence recovery after probe-induced dewetting, FRAP-ID). Upon surface tension evaluation via regular AFM-force spectroscopy, controlled AFM indentations induce dry spots in fluorescent condensates on a glass coverslip. The subsequent rewetting exhibits a contact line velocity that is used to quantify the condensed-phase viscosity. Therefore, in contrast with fluorescence recovery after photobleaching (FRAP), where molecular diffusion is observed, in FRAP-ID fluorescence recovery is obtained through fluid rewetting and the subsequent morphological relaxation. We show that the latter can be used to cross-validate viscosity values determined during the rewetting regime. Making use of fluid mechanics, FRAP-ID is a valuable tool to evaluate the mechanical properties that govern the dynamics of biomolecular condensates and determine how these properties impact the temporal aspects of condensate functionality.

A novel combined collector for high-performance flotation of cassiterite: Experimental insights and MD simulations

Collectors are critical in the flotation and separation of fine-grained minerals. In this study, a new combined collector, namely phosphoric acid (SPA)/dodecylbenzene sulfonate isopropanolamine (DBIA) was prepared via self-assembly. First, the flotation of cassiterite was investigated using SPA and DBIA separately, and the micro-collection mechanism of these single-material collectors on the surface of cassiterite was clarified by density functional theory calculations. Then, combined SPA/DBIA collectors were prepared, and the effect of the SPA/DBIA molar mass ratio on cassiterite flotation performance was studied. Surface tension measurements and molecular dynamics (MD) simulations were used to investigate the gas–liquid interfacial self-assembly of the SPA/DBIA collector. Subsequently, the flotation separation behavior of SPA/DBIA on the solid–liquid–gas interface was experimentally evaluated, and the adsorption mechanism of this combined collector at the three-phase interface was comprehensively investigated by performing MD simulations. The results show that SPA/DBIA combined collectors can obtain 80.88 % cassiterite flotation recovery at 1.2 × 10−4 mol/L. The addition of SPA led to the continuous adsorption of DBIA on the surface of cassiterite, forming a more stable and dense adsorption film. The mass density of the adsorption film was 319.27 ng/cm2, owing to the synergistic co-adsorption. Finally, the surface of the cassiterite was modified to enhance its hydrophobicity. This work demonstrates the application of collector self-assembly to improve the recovery of fine-grained cassiterite via flotation.

Influence of critical micelle concentration of choline-based long chain fatty acid soaps on their antibacterial activity against Methicillin resistant Staphylococcus aureus

HypothesisAntimicrobial resistance (AMR) is a pressing global health concern. ESKAPEE pathogens, such as Methicillin-resistant Staphylococcus aureus (MRSA) are notable of concern in healthcare settings due to their resistance to critical antibiotics. To combat AMR, the development of alternatives such as bacterial membrane-active agents is crucial. Fatty acids (FAs) have emerged as a sustainable, antibiotic-free solution with inherent antibacterial activity. However, long chain saturated fatty acids (LCFAs) sodium soaps exhibit poorly antibacterial properties in comparison to short chain FAs, believed to be linked to limited solubility in aqueous media. ExperimentsWe employed choline as a chaotropic organic counter-ion to enhance the solubility of LCFAs and investigated their antibacterial effects against MRSA. The optimal medium conditions for micelle formation for LCFAs was first investigated. Then, we determined the critical micelle concentration (CMC), micellar morphology, and aggregation number through surface tension measurements and small angle neutron scattering experiments. Antimicrobial activity was assessed using minimum bactericidal concentration (MBC) assays and time-kill experiments. FindingsWe have identified conditions where LCFAs are effective against MRSA for the first time, providing valuable insights for developing new antibacterial agents to fight AMR. LCFAs need to be used above their Krafft temperatures and CMC to exhibit antibacterial efficacy.

Surface light scattering: the capability of precisely measuring the interfacial properties of Newtonian fluids within the capillary wave transition region

This work employs a theoretical power spectrum of the dynamics of surface fluctuations in the frequency domain to elucidate the dissipation of capillary waves of fluids in the near-critical oscillation or transition region, seeking to resolve the problem of large discrepancies in viscosity and surface tension measurements in the region. The frequency-domain analysis approach was suggested, involving the discrete Fourier transform to transform the time domain data to the frequency domain and the fitting algorithm for the power spectrum. A total of three refrigerants, four alkanes and six fatty esters were chosen to examine the approach, with a range of the dimensionless number Y between 1.3 and 101.9. The findings demonstrate that frequency-domain approach is an effective way of dealing with dissipation issues for surface light scattering method when approaching the critical oscillation region, and thus could extend the technique for determining the viscosity and surface tension of Newtonian fluids to a sufficient wide viscosity range.