Separation of interfacial processes

An alternative electrochemical approach to the measurement of fast interfacial kinetics exploits the use of the scanning electrochemical microscope (SECM). A schematic of this device is shown in Fig. 14 the principle of the method rests on the perturbation of the intrinsic diffusive flux to the microelectrode, described by Eq. (34) above. A number of reviews of the technique exist [109,110]. In the case of the L-L interface, the microelectrode probe is moved toward the interface once the probe-interface separation falls within the diffusion layer, a perturbation of the current-distance response is seen, which can be used to determine the rate of interfacial processes, generally by numerical solution of the mass-transport equations with appropriate interfacial boundary conditions. The method has been... 

The importance of mixing at a molecular level was emphasized by the study of mixing processes in which chemical reactions played an essential role. Investigations into combustion problems have been the most influential. In this particular example, because the chemistry is frequently very fast in comparison with other characteristic time scales, separation of the process into interfacial extension by large scale motions and interfacial reaction involving molecular transport was particularly evident. Perhaps the first clear statement of these ideas in an analytical framework is that of Marble Broadwell (1977), although the general intuitive decomposition of the problem in this manner is much older. 

The terminal R groups can be aromatic or aliphatic. Typically, they are derivatives of monohydric phenoHc compounds including phenol and alkylated phenols, eg, /-butylphenol. In iaterfacial polymerization, bisphenol A and a monofunctional terminator are dissolved in aqueous caustic. Methylene chloride containing a phase-transfer catalyst is added. The two-phase system is stirred and phosgene is added. The bisphenol A salt reacts with the phosgene at the interface of the two solutions and the polymer "grows" into the methylene chloride. The sodium chloride by-product enters the aqueous phase. Chain length is controlled by the amount of monohydric terminator. The methylene chloride—polymer solution is separated from the aqueous brine-laden by-products. The facile separation of a pure polymer solution is the key to the interfacial process. The methylene chloride solvent is removed, and the polymer is isolated in the form of pellets, powder, or slurries. 

Foam Production This is important in froth-flotation separations in the manufac ture of cellular elastomers, plastics, and glass and in certain special apphcations (e.g., food products, fire extinguishers). Unwanted foam can occur in process columns, in agitated vessels, and in reactors in which a gaseous product is formed it must be avoided, destroyed, or controlled. Berkman and Egloff (Emulsions and Foams, Reinhold, New York, 1941, pp. 112-152) have mentioned that foam is produced only in systems possessing the proper combination of interfacial tension, viscosity, volatihty, and concentration of solute or suspended solids. From the standpoint of gas comminution, foam production requires the creation of small biibbles in a hquid capable of sustaining foam. 

Since some structural and dynamic features of w/o microemulsions are similar to those of cellular membranes, such as dominance of interfacial effects and coexistence of spatially separated hydrophilic and hydrophobic nanoscopic domains, the formation of nanoparticles of some inorganic salts in microemulsions could be a very simple and realistic way to model or to mimic some aspects of biomineralization processes [216,217]. 

As this volume attests, a wide range of chemistry occurs at interfacial boundaries. Examples range from biological and medicinal interfacial problems, such as the chemistry of anesthesia, to solar energy conversion and electrode processes in batteries, to industrial-scale separations of metal ores across interfaces, to investigations into self-assembled monolayers and Langmuir-Blodgett films for nanoelectronics and nonlinear optical materials. These problems are based not only on structure and composition of the interface but also on kinetic processes that occur at interfaces. As such, there is considerable motivation to explore chemical dynamics at interfaces. 

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