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Surfactant reverse

Figure 8.6—Effect of a cationic surfactant reversing the polarity of the capillary inner wall. Because the migration of analytes must always be in the direction of the detector, the voltage polarity of the instrument must be reversed in order for anionic species to move towards the anode, thus towards the detector. Figure 8.6—Effect of a cationic surfactant reversing the polarity of the capillary inner wall. Because the migration of analytes must always be in the direction of the detector, the voltage polarity of the instrument must be reversed in order for anionic species to move towards the anode, thus towards the detector.
Cationic surfactants Reverse charge on capillary wall... [Pg.159]

AV Levashov, NL Klyachko, NG Bogdanova, K Martinek. FEBS Lett 268 238-240, 1990. NG Bogdanova. Enzyme Catalysis in Surfactant Reverse Micellar Systems Solvated with Water-Organic Solvent Mixtures. PhD dissertation, Moscow State University, Russia, 1989. NL Klyachko, S Merker, K Martinek, AV Levashov. Dokl Akad Nauk SSSR (Russ) 298 1479-1481, 1988. [Pg.380]

The alternative use of cationic surfactants (quaternary alkylammonium salts) is recommended to increase retention of highly hydrophilic compounds. Cationic surfactants reverses the EOF. As the cationic micelles migrate electrophoretically against the anodic EOF, an extended migration window results. An example of MEKC separation using cationic surfactants is the analysis... [Pg.915]

The wide range of applications and increasing interests on the studies of nonionic surfactant reverse micelles or W/O microemulsions has shown their significance in colloid and polymer sciences. Due to biocompatibilily and biodegradability of the glycerol-based nonionic surfactants, studies on the self-assemblies of these surfactants in polar and nonpolar solvents offer various practical applications in the food, cosmetics, and pharmaceutical industries. [Pg.53]

This chapter has shown a possible route to the free structural control of glycerol-based nonionic surfactants reverse micelles, and it is found that the solvent properties, temperature, composition, chain length of surfactant and headgroup size, and water can be the tunable parameters for the structural variation of reverse micelles. [Pg.54]

In this paper, the results of a Monte Carlo method for the simulation of the stochastic time evolution of the micellization process are presented. The computational algorithm [1] used represents an optimization of a general procedure introduced by Gillespie some years ago [2]. It was applied to the case of surfactant reversible association according to the general mechanism reported in Fig. 1 that allows associations and dissociations among -mers of whatever aggregation number. [Pg.161]

Association colloids Homogeneous, thermodynamically stable solutions of spontaneous self-assembled surfactant aggregates micelles, typically composed of single-tailed surfactants reversed micelles in oil with water pools, vesicles typically composed of twin-tailed surfactants and microemulsions composed of at least oil, water, and surfactant and also with alcohols, either aqueous (oil-in-water droplets), bicontinuous (no droplets), or reverse (water-inoil droplets). [Pg.3764]

Keywords Cationic surfactants, reverse aggregate of Interfacial water, structure of Reverse micelles Water-in-oil microemulsions... [Pg.101]

The influence of micellar solubilization on co-crystal eutectic points is presented in Table 11.2 for carbamazepine-salicylic acid (CBZ-SLC) in aqueous media. Addition of surfactant reverses the co-former to drug molar concentration ratios at the eutectic. In the absence of surfactant, [SLC]e > [CBZ]e , indicating that the co-crystal requires excess co-former to be at equilibrium with pure drug. This situation is reversed in 35 mM (1%) SLS solution, where [CBZ]eu > [SLC]eu demonstrating that there is a CSC at SLS concentrations below 1 %. [Pg.272]

Abstract The enzymatic polymerization of ADP was carried out in sodium bis(2-ethylhexyl)sulfosuccinate (AOT)-reversed micellar solutions. The poly (adenylic acid), poly(A), being formed in the water pools precipitated out of the AOT solution together with the enzyme, whose activity was maintained for a long time. The process of the precipitation was studied in comparison with the polymerization in cationic surfactant reversed micelles and the precipitate aggregates were observed by atomic force microscopy (AFM). [Pg.256]

A number of other reports have been made relating to the use of surfactants, reverse micelles, microemulsions, membranes and polyelectrolytes for the synthesis of noble metal nanoparticles [157-159]. This type of synthetic method generally involves a two-phase system with a surfactant causing the formation of a microemulsion or micelle, and maintains a favorable microenvironment together with extraction of metal ions from aqueous phase to organic phase. In such cases, the surfactant not only acts as a stabilizer but also plays an important role in controlling crystal growth. [Pg.437]

Li WZ, Chen WM, Kobayashi T. Aerosolised surfactant reverses respiratory failure in lung lavaged rats. Acta Anaesthesiol Scand 1994 38 82-88. [Pg.220]


See other pages where Surfactant reverse is mentioned: [Pg.259]    [Pg.43]    [Pg.45]    [Pg.3096]    [Pg.403]    [Pg.165]    [Pg.1452]    [Pg.471]    [Pg.2072]    [Pg.388]    [Pg.256]    [Pg.257]    [Pg.1939]    [Pg.1939]    [Pg.2810]    [Pg.515]   
See also in sourсe #XX -- [ Pg.602 ]




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