Electrostatic adsorption, application

The application of the SEA approach to other systems is straightforward, and involves the three steps (PZC determination, uptake-pH survey, and tuned reduction) demonstrated in the earlier sections. It has recently been suggested that electrostatic adsorption over silanol groups is the cause for metal overexchange in low-aluminum zeohtes [61], It is presently being employed to study noble metal uptake on pure oxides of titania, ceria, zirconia, and niobia. 

With the application of protein microarrays in mind, Spencer and coworkers immobilized poly(lysine) with grafted PEG side chains on various metal or semiconductor oxide surfaces via electrostatic adsorption [200], Part of the PEG side chain was functionalized with biotin at the distal end. Streptavidin was bound to the surface-tethered biotin in a subsequent step, and the remaining unoccupied binding pockets of streptavidin were then used to immobilize biotinylated capture antibodies. As an example of an immunoassay, biotinylated goat anti-rabbit IgG was immobilized, which then specifically bound rabbit IgG. 

Application of the Electrostatic Adsorption Models to Natural Systems... 

Unlike supported metal oxides, which can be prepared with high dispersion in many cases simply by calcining mixtures of bulk oxide and support, it appears that well-dispersed metals are most easily produced from well-dispersed metal precursors. Once deposited in this fashion, an appropriately mild reduction treatment will preserve the high dispersion of the precursor in the reduced metal particles. This chapter will demonstrate that a simple method based on electrostatic adsorption, employing common, relatively cheap precursors, is widely applicable to synthesize highly dispersed metals on simple supports, metals highly dispersed onto a supported promoter, and highly dispersed bimetallic catalysts. 

It is of special interest for many applications to consider adsorption of fiuids in matrices in the framework of models which include electrostatic forces. These systems are relevant, for example, to colloidal chemistry. On the other hand, electrodes made of specially treated carbon particles and impregnated by electrolyte solutions are very promising devices for practical applications. Only a few attempts have been undertaken to solve models with electrostatic forces, those have been restricted, moreover, to ionic fiuids with Coulomb interactions. We would hke to mention in advance that it is clear, at present, how to obtain the structural properties of ionic fiuids adsorbed in disordered charged matrices. Other systems with higher-order multipole interactions have not been studied so far. Thermodynamics of these systems, and, in particular, peculiarities of phase transitions, is the issue which is practically unsolved, in spite of its great importance. This part of our chapter is based on recent works from our laboratory [37,38]. 

It is assumed that the quantity Cc is not a function of the electrolyte concentration c, and changes only with the charge cr, while Cd depends both on o and on c, according to the diffuse layer theory (see below). The validity of this relationship is a necessary condition for the case where the adsorption of ions in the double layer is purely electrostatic in nature. Experiments have demonstrated that the concept of the electrical double layer without specific adsorption is applicable to a very limited number of systems. Specific adsorption apparently does not occur in LiF, NaF and KF solutions (except at high concentrations, where anomalous phenomena occur). At potentials that are appropriately more negative than Epzc, where adsorption of anions is absent, no specific adsorption occurs for the salts of... 

Electrochemical techniques have been utilized for many years to study metal corrosion. Two of these techniques, linear polarization (LP) and cyclic voltammetry (CV), complement each other, LP providing corrosion rates under conditions where the surface is minimally altered and CV furnishing information about the corrosion mechanism. With the advent of impedance spectroscopy (IS), both kinds of information can be gleaned simultaneously and more rapidly, while leaving the surface almost intact. In this paper, we discuss the application of IS to the study of rapid steel corrosion and describe a study we undertook to elucidate the roles played by adsorption and film formation in the inhibition mechanisms of the above-named compounds. For comparison, we also investigated two quaternary nitrogen salts, which appear to adsorb electrostatically and presumably do not form macroscopic films (8). 

Nucleic acids, DNA and RNA, are attractive biopolymers that can be used for biomedical applications [175,176], nanostructure fabrication [177,178], computing [179,180], and materials for electron-conduction [181,182]. Immobilization of DNA and RNA in well-defined nanostructures would be one of the most unique subjects in current nanotechnology. Unfortunately, a silica surface cannot usually adsorb duplex DNA in aqueous solution due to the electrostatic repulsion between the silica surface and polyanionic DNA. However, Fujiwara et al. recently found that duplex DNA in protonated phosphoric acid form can adsorb on mesoporous silicates, even in low-salt aqueous solution [183]. The DNA adsorption behavior depended much on the pore size of the mesoporous silica. Plausible models of DNA accommodation in mesopore silica channels are depicted in Figure 4.20. Inclusion of duplex DNA in mesoporous silicates with larger pores, around 3.8 nm diameter, would be accompanied by the formation of four water monolayers on the silica surface of the mesoporous inner channel (Figure 4.20A), where sufficient quantities of Si—OH groups remained after solvent extraction of the template (not by calcination). 

Electrostatic fluidized-bed coating, 7 55-56 Electrostatic forces, 9 569, 570 11 800 and adsorbent selectivity, 1 584 in adsorption, 1 583 in solvent-solute interactions, 23 91-92 Electrostatic particle forces, in depth filtration theory, 11 339 Electrostatic precipitators (ESP), 11 714 13 180 23 552 26 699-706 advantages of, 26 700 applications of, 26 701-703, 705t design considerations related to,... 

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