Tetradecyltrimethylammonium Bromide Research Articles

Strain engineering of Bi2S3 microspheres via organic intercalation enabled high performance sodium storage

Conversion or alloying-type layered metal chalcogenides, which hold great promise as anodes for sodium storage, encounter a significant challenge of volume expansion due to the accumulation of inner strain during the charge–discharge process. This issue leads to severe stress concentration and necessitates urgent attention in terms of dispersing the distribution of inner strain through advanced strain engineering techniques. In this study, we have successfully fabricated Bi2S3-TTAB microspheres composed of Bi2S3 nanorods intercalated with tetradecyltrimethylammonium bromide (TTAB). By periodically inserting the soft TTAB into the interlayer of Bi2S3, we effectively isolate and confine the Bi2S3 layers while simultaneously expanding the interlamellar spacing. This innovative approach disperses and alleviates the inner strain of Bi2S3 at an atomic level, thereby ensuring electrode stability. As a competitive conversion-alloying-type anode for sodium-ion batteries, the Bi2S3-TTAB microspheres demonstrate remarkable performance in terms of high rate capacities and cycle stability (208.4 mAh g−1 at 15 A g−1; 4910 cycles at 10 A g−1 with 87.8 % capacity retention). This exceptional Na-ion storage capability enables the utilization of Bi2S3-TTAB combined with active carbon as an advanced sodium ion capacitor that demonstrates impressive energy and power densities (144.0 Wh kg−1 and 5.0 kW kg−1).

Surface-active ionic liquids as drug carriers: A physico-chemical study

This work evaluates the potential of two surface active ionic liquids (SAILs) 1-dodecyl-3-methylimidazolium bromide and 1-tetradecyl-3-methylimidazolium bromide as drug carrier for ciprofloxacin (CPF) and compares them with their conventional counterparts dodecyltrimethylammonium bromide and tetradecyltrimethylammonium bromide using spectroscopic and electrochemical techniques. Different physico-chemical parameters including critical micelle concentration (CMC), binding constants, partition coefficients and their corresponding free energy changes, thermodynamic parameters of micellization and redox behavior of micelle-drug systems were investigated. Both the SAILs demonstrated higher solubilization powers and binding constants owing to the less polar nature of imidazolium ring. Lower CMCs indicated relatively stronger hydrophobic forces existing in all SAILs-CPF systems tested. The cyclic voltammetry displayed shifting of oxidation peaks towards higher positive potential in the micellar region indicating the protection of CPF against oxidation. This work demonstrates the benefits of using SAILs as drug carriers due to their lower CMCs, improved binding and partition coefficients, and favorable electrochemical results.

Effects of short-chain alcohols and urea on the association of tetradecyltrimethylammonium bromide surfactant and cefixime trihydrate antibiotic: Conductometric and physicochemical analysis

This study explores the interaction of tetradecyltrimethylammonium bromide (TTAB), with an antibiotic drug, cefixime trihydrate (CMT), with a particular focus on conductivity changes as a reliable indicator of micelle formation. Influence of various alcohols (methanol (MeOH), ethanol (EtOH), 1-propanol (1-PrOH), 2-propanol (2-PrOH)), and urea on the physicochemical properties for micellization of TTAB in aq. alcohols/urea solutions of CMT was investigated. As the concentration of alcohol and urea increases, the critical micelle concentration (CMC) undergoes a notable rise, while the degree of counterion binding (β) shows a decreasing trend as a function of [alcohols]/[urea]. Elevated temperatures impede the creation of micelles, directing to an increase in the CMC, thus necessitating a higher surfactant concentration for micelle development. The alterations in free energy (∆Gmo), enthalpy (∆Hmo), entropy (∆Smo), and molar heat capacity (∆Cm0) were analyzed to evaluate the feasibility and driving forces behind the process of micelle development. The negative values of ∆Gmo indicate that the formation of micelles in the system being studied occurs spontaneously. The ∆Hmo and ∆Smo values suggest the existence of electrostatic forces (ion-dipole and H-bonding) between the components (TTAB, CMT, and alcohol) in aq. MeOH media. In contrast, hydrogen bonding, electrostatic forces, and hydrophobic interactions are involved in the solutions of the other three alcohols and urea medium. The thermodynamic parameters of transfer (∆Gm,tr0, ∆Hm,tr0, and ∆Sm,tr0) and enthalpy-entropy compensation variables were computed and discussed for TTAB micelles in the presence of CMT drug in employed solvents. The discoveries hold significant implications for drug formulation and industrial processes concerning surfactants and additives, providing valuable insights for optimizing their performance and properties.

Highly selective ion precipitation flotation for ternary Co–Zn–Mn separation: Stepwise chelation capture of Co and Zn from simulated zinc hydrometallurgy wastewater

Ion precipitation flotation technology was demonstrated to be an efficient method for the separation of valuable metals from low-concentration solution. However, the selective separation of three metals from mixing solution is a great challenge, and highly selective reagents are the key to polymetallic separation. In this work, stepwise separation of Co and Zn from the simulated zinc hydrometallurgy wastewater containing ternary Co–Zn–Mn metals by ion precipitation flotation process was proposed. It's demonstrated that organic reagents of 1-nitroso-2-naphthol (NN) and sodium dimethyldithiocarbamate (SDDC) had excellent selectivity for the capture of Co and Zn to form respective precipitate from wastewaters via the chelation reactions. After precipitation, dodecylpyridinium chloride (DPC) and tetradecyltrimethylammonium bromide (TTAB) were chosen as surfactants for the separation of Co and Zn sediments from the solution via the flotation process. The effects of solution pH, molar ratio, reaction temperature, and reaction time on the selective precipitation efficiencies of Co and Zn as well as the effects of surfactant dosage and flotation gas velocity on the flotation separation efficiencies were systematically investigated. It's demonstrated that the comprehensive recovery rates of Co, Mn, and Zn reach 98%, 90%, and 99%, respectively. After separation, oxidation calcination of the foam products was conducted to prepare high-purity Co3O4 and ZnO nanoparticles in which the organic matters were burnt out with gas emissions. The stepwise chelation capture mechanisms of Co and Zn by highly selective precipitation reagents were minutely discussed. It's demonstrated that the proposed selective stepwise precipitation and flotation method is suitable for recovery of critical metal ions from low-concentration polymetallic wastewaters.

Self‐assembly and solution behavior of cationic surfactants in water‐trifluoroethanol environment: An experimental and theoretical approach

AbstractThe micellization behavior of conventional cationic surfactant: tetradecyltrimethylammonium bromide (TTAB), and Gemini surfactant (GS): N,N′‐ditetradecyl‐N,N,N′,N′‐tetramethyl‐N,N′‐ethanediyl‐diammonium dibromide (14‐2‐14) in water and water‐trifluoroethanol (TFE) solvent mixture has been examined using tensiometric and small‐angle neutron scattering (SANS) techniques. Critical micelle concentration (CMC), and various interfacial parameters such as surface tension at CMC (γCMC), surface pressure at CMC (πCMC), maximum surface excess concentration (Γmax), and minimum area occupied by the head group (Amin) were evaluated for our examined systems at 303.15 K. It was observed that with the increase in TFE concentration, the CMC of the tested cationic surfactants decreased, thereby favoring the micellization in the presence of the surface‐active TFE. Furthermore, the geometry and aggregation number (Nagg) of surfactant micelles were inferred using SANS that revealed the decrease in micelle size of cationic surfactants. Additionally, the computational simulation study provided an insight into the molecular interactions in the examined system that validated our experimental findings.

Reproductive Toxicities of Tetradecyltrimethylammonium Chloride and Tetradecyltrimethylammonium Bromide on Caenorhabditis elegans over Four Consecutive Generations

Reproductive Toxicities of Tetradecyltrimethylammonium Chloride and Tetradecyltrimethylammonium Bromide on Caenorhabditis elegans over Four Consecutive Generations

Assessment of the assembly behaviour and physicochemical parameters for the tetradecyltrimethylammonium bromide and promazine hydrochloride mixture: Impact of monohydroxy organic compounds

Assessment of the assembly behaviour and physicochemical parameters for the tetradecyltrimethylammonium bromide and promazine hydrochloride mixture: Impact of monohydroxy organic compounds

Role of Alkyl Chain Length in Surfactant-Induced Precipitation of Reactive Brilliant Blue KN-R

To develop a cost-effective method for the effective removal of reactive brilliant blue KN-R (RBB KN-R) from wastewater, we investigated the interactions between RBB KN-R and three cationic surfactants with different alkyl chain lengths, namely dodecyltrimethylammonium bromide (DTAB), tetradecyltrimethylammonium bromide (TTAB), and cetyltrimethylammonium bromide (CTAB). Employing a conductivity analysis, surface tension analysis, ultraviolet-visible spectrophotometry, and molecular dynamics simulation, we ascertained that RBB KN-R formed a 1:1 molar ratio dye–surfactant complex with each surfactant through electrostatic attraction. Notably, an augmentation in alkyl chain length correlated with increased binding strength between RBB KN-R and the surfactant. The resulting dye–surfactant complex exhibited heightened surface activity, enabling interactions through hydrophobic forces to generate dye–surfactant aggregates when the molar ratio was below 1:1. Within these mixed aggregates, self-assembly of RBB KN-R molecules occurred, leading to the formation of dye aggregates. Due to the improved hydrophobicity with increased alkyl chain length, TTAB and CTAB could encapsulate dye aggregates within the mixed aggregates, but DTAB could not. The RBB KN-R aggregates tended to distribute on the surface of the RBB KN-R-DTAB mixed aggregates, resulting in low stability. Thus, at a DTAB concentration lower than CMC, insoluble particles readily formed and separated from surfactant aggregates at an RBB KN-R and DTAB molar ratio of 1:4. Analyzing the RBB KN-R precipitate through scanning electron microscopy (SEM) and Fourier transform infrared spectroscopy (FTIR) and measuring the DTAB concentration in the supernate revealed that, at this molar ratio, all RBB KN-R precipitated from the dye–surfactant mixed solution, with only 7.5 ± 0.5% of DTAB present in the precipitate. Furthermore, the removal ratio of RBB KN-R reached nearly 100% within a pH range of 1.0 to 9.0 and standing time of 6 h. The salt type and concentration did not significantly affect the precipitation process. Therefore, this simultaneous achievement of successful RBB KN-R removal and effective separation from DTAB underscores the efficacy of the proposed approach.

Study on the association and phase separation behavior of surfactants and promethazine hydrochloride: impact of ammonium electrolytes.

In the current study, the association and phase separation of cationic tetradecyltrimethylammonium bromide (TTAB) and nonionic Triton X-100 (TX-100) surfactants with promethazine hydrochloride (PMH) were investigated in aqueous ammonium-based solutions. The micellization nature of the TTAB and PMH drug mixture was examined by evaluating critical micelle concentration (CMC) and counterion binding extent (β) at different salt contents and temperatures (298.15-323.15 K). Micelle formation in the TTAB + PMH mixture was enhanced in the presence of ammonium salts, whereas the process was delayed with an increase in temperature in the respective salt solution. With an increase in salt content, the cloud point (CP) of the TX-100 + PMH mixture decreased, which revealed that the respective progression occurred through the salting out phenomenon. In micellization and clouding processes, the changes in free energies ΔG0m and ΔG0c were found to be negative and positive, respectively, demonstrating that the corresponding processes are spontaneous and non-spontaneous. Standard enthalpies (ΔH0m/ΔH0c) and standard entropies (ΔS0m/ΔS0c) for the association and clouding processes, respectively, were also calculated and discussed. The core forces amid TTAB/TX-100 and PMH in the manifestation of electrolytes are dipole-dipole and hydrophobic forces among the employed components according to the values for ΔH0m/ΔH0c and ΔS0m/ΔS0c, respectively.

Molecular interactions of cationic/anionic surfactants in presence of anionic antibiotic drug cloxacillin sodium at different temperatures: Micellization and thermodynamic studies

The physicochemical properties and interactions of surfactant–drug aggregates are regarded as essential features to achieve optimum therapeutic action of the drug. In this article, the effect of various concentrations of anionic antibiotic drug cloxacillin sodium (ClxNa) on the micellization of cationic surfactants such as cetyltrimethylammonium bromide (CTAB), tetradecyltrimethylammonium bromide (TTAB) and anionic surfactant sodium dodecyl sulphate (SDS) have been investigated using electrical conductance measurement at different temperatures (288.15 K, 293.15 K, 298.15 K, 303.15 K, 308.15 K, and 313.15 K). The results suggest an increase in critical micelles concentration (CMC) values for cationic surfactants (CTAB/TTAB) with a rise in drug concentration (0 mM up to 10 mM) whereas anionic surfactant SDS shows a decrease in CMC at higher drug concentrations (from 2.5 mM up to 10 mM) at all the studied temperatures. The degree of counterion dissociation (α) values for TTAB aggregates show a slight increase with [ClxNa], except at a few lower temperature ranges whereas such a regular trend was not obtained for CTAB and SDS aggregates. Temperature-dependent CMC values show a nonlinear nature with a rise in temperatures and follow a U-shaped curve for all studied pure surfactant and surfactant–ClxNa systems. Micellization for all surfactant-drug systems is found to be spontaneous. Investigation of other temperature-dependent thermodynamic parameters such as change in standard enthalpy (ΔHm0), and entropy (ΔSm0) of micellization suggest that surfactant–drug interactions are both endothermic (ΔHm0 < 0, particularly at lower temperatures) and exothermic (ΔHm0 < 0, at higher temperatures), whereas micellization is largely entropically driven (ΔSm0 > ΔHm0).

Vesicle-to-micelle transition in a double chain quaternary ammonium surfactant system: Interfacial behavior and molecular insights

Vesicles have emerged as promising drug carriers with excellent compatibility with cell membranes, holding immense potential for biomedical applications. While most reported micelle-to-vesicle transitions involve increasing surfactant or additive concentrations, the reverse vesicle-to-micelle transition remains less explored. In this study, we investigate the vesicle-to-micelle transition of hexyldimethyloctylammonium bromide (C6C8Br) using dynamic light scattering, transmission electron microscopy, and fluorescence spectroscopy. Tetradecyltrimethylammonium bromide (TTABr), a single-chain tetraalkylammonium surfactant with the same chain-length, is studied for comparison. Through the chemical trapping (CT) method, we explore the interfacial composition changes during the vesicle-to-micelle transition. Notably, C6C8Br exhibits a unique characteristic setting it apart from TTABr and other cationic surfactants. At lower concentration ranges, there is a simultaneous increase in interfacial molarities of water and bromide ions, signifying a decrease in interfacial headgroup molarity and surfactant molecule packing. Moreover, our dissipative particle dynamics (DPD) simulation results show that, as the surfactant concentration rises, the interior angle between surfactant chains widens, and the molecular configuration of C6C8Br approaches a straight line. These combined CT and DPD findings underscore the prominent role of steric effects arising from the rigidity of the double-chain. These effects become more pronounced at higher C6C8Br concentrations, leading to looser interfacial packing of surfactant monomers and driving the transition from vesicles to micelles. Interestingly, the breakage of vesicles was not observed when replacing the counterion of C6C8Br with acetate in C6C8Ac solutions. CT results suggest that the elevated interfacial acetate molarity may faciliate the compact packing of surfactant monomers and hinder vesicle-to-micelle transformation. Our study provides a molecular-level understanding of the vesicle-to-micelle transitions in C6C8Br solutions and establishes a theoretical basis for morphological control of surfactant aggregates.

Interaction between gastric enzyme pepsin and tetradecyltrimethylammonium bromide in presence of sodium electrolytes: Exploration of micellization behavior

Pepsin is a proteolytic enzyme used in the treatment of digestive disorders. In this study, we investigated the physicochemical properties of the tetradecyltrimethylammonium bromide (TTAB) and pepsin protein mixture in various sodium salt media within a temperature range of 300.55–320.55 K with 5 K intervals. The conductometric study of the TTAB+pepsin mixture revealed a reduction in the critical micelle concentration (CMC) in electrolyte media. The micellization of TTAB was delayed in the presence of pepsin. The CMC of the TTAB + pepsin mixture was found to depend on the concentrations of electrolytes and protein, as well as the temperature variations. The aggregation of the TTAB+pepsin mixture was hindered as a function of [pepsin] and increasing temperatures, while micellization was promoted in aqueous electrolyte solutions. The negative free energy changes (∆Gm0) indicated the spontaneous aggregation of the TTAB+pepsin mixture. Changes in enthalpy, entropy, molar heat capacities, transfer properties, and enthalpy-entropy compensation variables were calculated and illustrated rationally. The interaction forces between TTAB and pepsin protein in the experimental solvents were primarily hydrophobic and electrostatic (ion-dipole) in nature. An analysis of molecular docking revealed hydrophobic interactions as the main stabilizing forces in the TTAB-pepsin complex.

Aggregation phenomena and physico-chemical properties of tetradecyltrimethylammonium bromide and protein (bovine serum albumin) mixture: Influence of electrolytes and temperature

It is important for biological, pharmaceutical, and cosmetic industries to understand how proteins and surfactants interact. Herein, the interaction of bovine serum albumin (BSA) with tetradecyltrimethylammonium bromide (TTAB) in different inorganic salts (KCl, K2SO4, K3PO4.H2O) has been explored through the conductivity measurement method at different temperatures (300.55 to 325.55 K) with a specific salt concentration and at a fixed temperature (310.55 K) using different salts concentrations. The extent of micelle ionization (α) and different thermodynamic parameters associated with BSA and TTAB mixtures in salt solutions were calculated. Evaluation of the magnitudes of ∆Hm0 and ∆Sm0 showed that the association was exothermic and primarily an enthalpy-operated process in all cases at lower contents of BSA, but the system became endothermic, and entropy driven in the presence of K3PO4.H2O at a relatively higher concentration of BSA. The enthalpy–entropy compensation variables were determined, which explained the types and nature of interactions between TTAB and BSA in salt media. Molecular docking analysis revealed that the main stabilizing factors in the BSA-TTAB complex are electrostatic and hydrophobic interactions. These findings aligned with the significant results obtained from the conductometry method regarding the nature and characteristics of binding forces observed between BSA and TTAB.

The micellization of tetradecyltrimethylammonium bromide and cefixime trihydrate mixture: investigation of the effects of sodium-based electrolytes and temperatures on the physico-chemical parameters and interaction forces

ABSTRACT This study exposes the influence of sodium electrolytes and temperature on the interaction forces between tetradecyltrimethylammonium bromide (TTAB) and antibiotic cefixime trihydrate (CMT). The results highlight the significance of considering temperature (from 300.55 to 320.55 K) and electrolytes (NaBr, Na2SO4, Na3PO4, and CH3COONa (NaOAc)) effects when designing drug formulations. Conductometric method was utilised to compute and understand physicochemical parameters occurring during drug-surfactant micellization. The addition of sodium electrolytes favours the micellization of the TTAB and CMT system in aq. salts solution (a decrease of CMC was acquired) except at higher NaOAc concentrations. In all the solvents used herein, the CMC values were detected to be increased with the escalation of working temperature. The and expose the survival of hydrophobic interaction involving TTAB and CMT drug in aq. medium whereas both electrostatic and hydrophobic interaction are in function in aq. salts medium. As an extension of the thermodynamic assessment, the molar heat capacity were estimated and discussed. The thermodynamics of transfer (, , and ) and enthalpy-entropy compensation parameters for TTAB + CMT micelles were also analysed. This comprehension of drug-surfactant interaction holds utmost significance in the development of efficient drug formulations and the optimisation of drug delivery techniques.

Micellization of a cationic and an anionic surfactant in the presence of diphenylcarbazide in aqueous media and the effect of micelle surface charge on the complexation of the solubilised ligand with metal ions

ABSTRACT In the present study, we carried out conductometric and surface tension analyses to report the critical micelle concentration (CMC) of tetradecyltrimethyl ammonium bromide (TTAB) and sodium dodecyl sulphate (SDS) as a function of the concentration of a diphenylcarbazide (DPC). It is found that the micellization of TTAB becomes unfavourable while that of SDS becomes favourable in the presence of DPC. This indicates a substantial difference in the mutual interaction of the sparingly soluble ligand with the cationic and the anionic surfactants. The complexation ability of the solubilised DPC with hydrated Zn(II) and Cd(II) ions at varying concentrations of the cationic and anionic surfactants was studied by UV–Vis spectral analyses. With increasing the concentration of both surfactants up to their respective CMC values, the absorbance of the metal–DPC complex increases. However, the absorbance of the complex in TTAB micelles sharply decreases, showing almost zero values beyond the CMC, but that in SDS remains almost steady with increasing the concentration of the surfactant, as evidenced from the visible spectra.

A study on surfactant modified polypyrrole nanostructures and its applications in supercapacitors

Nanocomposites of Polypyrrole (Ppy), were synthesized by chemical oxidative polymerization of pyrrole, in the presence of mono and mixed‐surfactant solutions using ammonium persulfate as an oxidant and were investigated for its applications in super capacitors. The surfactants used in the experiments included anionic surfactants, sodium dodecyl sulfate (SDS) and sodium dodecylbenzenesulfonate (SDBS) and cationic surfactants, tetradecyltrimethylammonium bromide (TTAB) as well as cetyltrimethylammonium bromide (CTAB). The morphology and structure of the resulting Ppy were investigated in detail with FESEM and FTIR, respectively. The addition of anionic surfactants produced globular morphology. The results showed that the interaction between the different surfactants and the interaction between the surfactants and the polymer influenced the morphology, structure and conductivity of the resulting polymer to different degrees. Apart from these, XRD, UV-Vis spectroscopy and cyclic voltammetry (CV) were also performed to characterize the prepared composites. In comparison with the results for mono surfactant solutions, the polymerization of pyrrole in mixed‐surfactant solutions shows significant changes in morphologies and electrochemical properties of Ppy. The results of CV show that the specific capacitance values of Ppy samples with anionic surfactants are greater than cationic surfactants. In case of mixed surfactants, sample with SDBS + TTAB posses highest specific capacitance of 204 Fg−1 at scan rate 100 mVs−1. The good electrochemical properties can be attributed to the highly porous structural advantage of the Ppy sample prepared using SDBS + TTAB. It indicates the energy holding capacity or capacitance of the prepared samples and can be utilized in sensing applications like supercapacitors.

Scraping of foam on a substrate

Hypothesis: Foam is not only an industrially important form of matter, but also one of soft jammed system such as colloidal suspensions and emulsion suspensions. Since foams are composed of gas bubbles and liquid, it is expected that the coupling of bubbles and liquid strongly affects rheology of foams, which is different from simple liquids. To reveal this coupling effect and considering the importance of foam applications, we studied the scraping of foam by a rigid plate on a substrate.Experiment: We mainly used 5.0 wt% solution of ionic surfactant TTAB (tetradecyltrimethylammonium bromide). We systematically investigate the scraping behaviors by the rigid plate as a function of scraping velocity, gap height, confinement length, amount of foam and wettability of the substrate.Findings: The results show that there are three distinguishable scraping patterns: homogeneous scraping, no scraping, and slendered scraping. These behaviors are clearly different from those of simple liquid systems. Of these, the upper limit of homogeneous scraping could be explained theoretically by the competition between dewetting and shear, which is not previously discussed. Furthermore, the theory is applicable to the scraping of other soft jammed systems such as colloidal and emulsion suspensions.

Analysis of Two Single and Three Double Long-Chain Quaternary Ammonium Compounds via Non-Aqueous Capillary Electrophoresis with Indirect Ultraviolet Detection

A novel method utilizing non-aqueous capillary electrophoresis (NACE) with indirect ultraviolet detection (IUD) has been developed for the analysis of five quaternary ammonium compounds (QACs). The QACs analyzed in this study include dodecyl trimethyl ammonium bromide, tetradecyl trimethyl ammonium bromide, dioctyl dimethyl ammonium chloride, octyldecyl dimethyl ammonium chloride and didecyl dimethy ammonium bromide. The separation process was carried out on an uncoated fused quartz capillary with a total length of 50.2 cm (effective length 40.0 cm) and a diameter of 50 μm. The separation buffer consisted of a mixture of MeOH/ACN (90:10, v/v) containing 2 mmol/L sodium acetate, 2 mmol/L trifluoroacetic acid (TFA) and 16 mmol/L dodecyl dimethyl benzyl ammonium chloride. The sample buffer utilized a mixture of MeOH/ACN (20:80, v/v) containing 2 mmol/L TFA. During analysis, a separation voltage of 7 kV was applied, resulting in a current of approximately 2.3 μA. The detection wavelength was set at 214 nm to ensure optimal sensitivity. Under optimal conditions, the method exhibited excellent performance characteristics, with a limit of detection of 0.5 mg/L and a limit of quantitation of 5.0 mg/L for the five QACs. Linear calibration curves were obtained in a concentration range of 5.0 to 100.0 mg/L, with correlation coefficients exceeding 0.999 for all compounds. The recoveries of the five QACs ranged from 92.3% to 114.7%, with relative standard deviations below 7.4%. To assess the applicability of the NACE-IUD method, 17 commercially available samples were successfully analyzed. The results confirmed the suitability of the method for accurate determination of the five QACs in disinfectant products. Notably, this method offers an environmentally friendly approach for the analysis of these QACs.

Equilibrium and dynamic surface properties of cationic/anionic surfactant mixtures based on alcohol ether sulfate

The equilibrium and dynamic surface properties of anionic surfactant alcohol ether sulfate with different EO distribution(C-AE2S and N-AE2S) and cationic surfactant tetradecyltrimethylammonium bromide (TTAB) mixtures under different molar ratios were investigated. Their surface activities, adsorption, and spreading performances were investigated by static/dynamic surface tension measurements, molecular dynamics simulation, and dynamic contact angle techniques at 298 K. The static surface tension analysis reveals that the critical micellization concentration (cmc) values and the surface tension at cmc (γ cmc) of the binary systems are much lower than that of the individual component. Compared with C-AE2S/TTAB, N-AE2S/TTAB systems have higher cmc and lower γ cmc. It was found from the molecular dynamics simulation that negative charges of C-AE2S were drastically neutralized by the positively-charged TTAB at the interface in the system of C-AE2S/TTAB. The dynamic surface tension results indicate that the adsorption process of aqueous solutions for both C-AE2S/TTAB and N-AE2S/TTAB are mixed diffusion-kinetic adsorption mechanisms. From the dynamic contact angle measurements, it could be obtained that the mixtures exhibit better spreading behavior than that of the individual component and N-AE2S/TTAB systems have lower contact angles than that of C-AE2S/TTAB at the same mixing ratios.

Isolation, Molecular Characterization and Mycochemical Analysis of Aspergillus quadrilineatus

Secondary metabolites of microbial origin, either as pure compounds or crude extracts, provide opportunities for new drug development because of their chemical diversity. The aim of the present study is to isolate Molecular characterization and extract the bioactive compounds from the fungus of A. quadrilineatus (OL979151) in the rhizospheric soil of sunflower and mustard crop fields in Davanagere region. Dilution plate technique was used to isolate the rhizosphere fungi. The total genomic DNA was extracted from isolate of Aspergillus quadrilineatus based on Cetrimide Tetradecyl Trimethyl Ammonium Bromide (CTAB). Mass production of the fungal mat of A. quadrilineatus was established on potato dextrose broth medium. The dried methanol extract of fungus was subjected to HR-LCMS analysis; Methanol extract of A. quadrilineatus fungus shows that the compounds Amobarbital, Pirbuterol, Bambuterol, Cilazaprilat, Oxotremorine, Aminopyrine and Oryzanol as the major constituents. The compounds exhibit analgesic, anti-inflammatory, and antipyretic properties and various therapeutic uses.