Cationic surfactants Applications

NMR measurements are very useful to understand the properties of the stabilizing reagents of metal nanoparticles. Author s group reported the structure of stabilization of non-ionic and cationic surfactants on platinum nanoparticles [22] and that of ternary amines on rhodium nanoparticles [23]. Such information is considerably important for applications of nanoparticles such as... 

The ITIES with an adsorbed monolayer of surfactant has been studied as a model system of the interface between microphases in a bicontinuous microemulsion [39]. This latter system has important applications in electrochemical synthesis and catalysis [88-92]. Quantitative measurements of the kinetics of electrochemical processes in microemulsions are difficult to perform directly, due to uncertainties in the area over which the organic and aqueous reactants contact. The SECM feedback mode allowed the rate of catalytic reduction of tra 5-l,2-dibromocyclohexane in benzonitrile by the Co(I) form of vitamin B12, generated electrochemically in an aqueous phase to be measured as a function of interfacial potential drop and adsorbed surfactants [39]. It was found that the reaction at the ITIES could not be interpreted as a simple second-order process. In the absence of surfactant at the ITIES the overall rate of the interfacial reaction was virtually independent of the potential drop across the interface and a similar rate constant was obtained when a cationic surfactant (didodecyldimethylammonium bromide) was adsorbed at the ITIES. In contrast a threefold decrease in the rate constant was observed when an anionic surfactant (dihexadecyl phosphate) was used. 

Wang and Pek [185] have described a simple titration method applicable to the analysis of cationic surfactants in sea water. Methyl orange and azure A were used as primary dye and secondary dye, respectively. The method is free from interference by high levels of inorganic salts in sea water. 

When the influence was studied of different surfactants on the CL intensity of the reaction of lucigenin with isoprenaline, it was found that while cationic surfactants such as HTAH and HTAB and anionic surfactants such as SDS decrease the CL signal, the presence of Brij-35 increases the signal by a factor of 2.1 compared to that obtained in an aqueous medium [61]. As a result, a quite sensitive analytical method has been established for determination of isoprenaline, using Brij-35 as a CL enhancer. Application of the method has been satisfactorily verified with the determination of isoprenaline in pharmaceutical preparations. 

Direct determination of surfactants in complex matrices can also be carried out using ion-selective electrodes. Depending on the membranes and additives used, the detergent electrodes are optimized for the detection of anionic surfactants [81], cationic surfactants [82], and even nonionic surfactants [83]. The devices are sensitive to the respective group of surfactants but normally do not exhibit sufficient stability and reproducibility for their use in household appliances. With further optimization of membrane materials, plasticizers and measurement technology, surfactant-selective electrodes offer high potential for future applications. 

Suppliers of visible spectrophotometers are reviewed in Table 1.1. Spectroscopic methods are applicable to the determination of phenols, chlorophenols, amines, mixtures of organics, boron, halogens, total nitrogen and total phosphorus in soils, cationic surfactants, carbohydrates, total nitrogen, phosphorus and sulphur in non-saline sediments, boron, total organic carbon, total sulphur and arsenic in saline sediments, cationic surfactants, adenosine triphosphate and total organic carbon in sludges. 

Cationic surfactants show a high affinity for negatively charged surfaces making them suitable for industrial applications and as components for consumer products where they are used as disinfectants, foam depressants, and first and foremost as textile softeners [23], Due to the possible formation of ion-pair associates they are usually not formulated together with anionic surfactants. 

DTDMAC was the first widely used cationic surfactant produced at the industrial scale since the 1960s. Its main application was as a fabric softening active agent. Due to its physico-chemical properties, largely determined by the positively charged head group and the long alkyl chains, it adsorbs onto fabrics and makes textiles feel soft. 

Numerous applications have been shown to exist that overcome the general problems of lack of volatility and instability at higher temperatures that principally hamper direct analysis of surfactants by GC methods. Thus, a whole suite of derivatisation techniques are available for the gas chromatographist to successfully determine anionic, non-ionic and cationic surfactants in the environment. This enables the analyst to combine the high-resolution chromatography that capillary GC offers with sophisticated detection methods such as mass spectrometry. In particular, for the further elucidation of the complex mixtures, which is typical for the composition of many of the commercial surfactant formulations, the high resolving power of GC will be necessary. 

These observations obtained from the application of different API techniques are determinative for qualitative and quantitative FIA results in the analysis of non-ionic and ionic surfactants. Therefore, both ionic surfactant types, anionic and cationic surfactant blends, besides a non-ionic AE surfactant blend were examined, recording their FIA-MS and MS-MS spectra from the blends before the spectra were generated from the mixture of all blends. The results, which show considerable variation, will be presented and discussed as follows. 

SPECTROMETRY—IX. LC-MS ANALYSES OF CATIONIC SURFACTANTS METHODS AND APPLICATIONS... 

The application of surfactants can enhance remediation or recovery of contaminants by increasing their mobility and solubility. Surfactants can thus be used to enhance ex situ soil washing, in situsoil flushing, non-aqueous-phase liquid (NAPE) pump-and-treat applications, and in situbiodegradation. Cationic surfactants have been shown to improve the capacity of soil... 

Asphalt emulsions are dispersions of asphalt in water that are stabilized into micelles with either an anionic or cationic surfactant. To manufacture an emulsion, hot asphalt is mixed with water and surfactant in a colloid mill that produces very small particles of asphalt on the order of 3 pm. These small particles of asphalt are prevented from agglomerating into larger particles by a coating of water that is held in place by the surfactant. If the asphalt particles agglomerate, they could setde out of the emulsion. The decision on whether a cationic or anionic surfactant is used depends on the application. Cationic stabilized emulsions are broken, ie, have the asphalt settle out, by contact with metal or silicate materials as well as by evaporation of the water. Since most rocks are silicate-based materials, cationic emulsions are commonly used for subbase stabilization and other similar applications. In contrast, anionic emulsions only set or break by water evaporation thus an anionic emulsion would be used to make a cold patch compound. 

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