Electric field enhancement mechanism

While the growth of thermal oxides is dominated by high-temperature diffusion of oxygen in the oxide matrix, anodic oxide growth is dominated by field-enhanced hydroxyl diffusion at RT. These different growth mechanisms result in pronounced differences in the morphological, chemical and electrical properties of the oxide. 

With capillary electrophoresis (CE), another modern primarily analytically oriented separation methodology has recently found its way into routine and research laboratories of the pharmaceutical industries. As the most beneficial characteristics over HPLC separations the extremely high efficiency leading to enhanced peak capacities and often better detectability of minor impurities, complementary selectivity profiles to HPLC due to a different separation mechanism as well as the capability to perform separations faster than by HPLC are frequently encountered as the most prominent advantages. On the negative side, there have to be mentioned detection sensitivity limitations due to the short path length of on-capillary UV detection, less robust methods, and occasionally problems with run-to-run repeatability. Nevertheless, CE assays have now been adopted by industrial labs as well and this holds in particular for enantiomer separations of chiral pharmaceuticals. While native cyclodextrins and their derivatives, respectively, are commonly employed as chiral additives to the BGEs to create mobility differences for the distinct enantiomers in the electric field, it could be demonstrated that cinchona alkaloids [128-130] and in particular their derivatives are applicable selectors for CE enantiomer separation of chiral acids [19,66,119,131-136]. 

Besides the field influence on the monomer reactivity ratio mentioned in the previous sections, living anionic systems present strong evidence against the electroinitiated polymerization mechanism. First of all, the experimental fact, that the apparent rate constant of propagation was increased by the presence of an electric field, rules out a possibility that the observed field-accelerating effect resulted only from the initiation reaction enhanced by the field. The finding that the field had no influence on the dependences of the polymerization rate on monomer and initiater concentrations, but did influence the rate constant, implies that the reaction mechanism was unaltered by the application of the field. These results confirm our very low opinion of the electroinitiated polymerization mechanism. 

Several theories have been proposed to explain the mechanisms involved in an AFID system (31). In general, thermal energy is required to atomize a particular alkali metal salt. The alkali metal atoms formed ionize and are subjected to an electric field. This produces a current proportional to the number of ions. The presence of halogen, phosphorus, and even nitrogen enhance the signal. The system is complex and does not lend itself to a complete theory as intricate surface phenomena are possible. In addition, there is speculation that photochemical processes occur and realization that combustion products formed in the flame can interact to form a multitude of species compound the difficulty. It has been proven that the process does depend on thermal energy and not strictly speaking on the products of combustion. For this reason many researchers prefer the term thermionic ionization. 

The balance over the ith species (equation IV. 5) consists of contributions from diffusion, convection, and loss or production of the species in ng gas-phase reactions. The diffusion flux combines ordinary (concentration) and thermal diffusions according to the multicomponent diffusion equation (IV. 6) for an isobaric, ideal gas. Variations in the pressure induced by fluid mechanical forces are negligible in most CVD reactors therefore, pressure diffusion effects need not be considered. Forced diffusion of ions in an electrical field is important in plasma-enhanced CVD, as discussed by Hess and Graves (Chapter 8). 

Proposed Mechanism Responsible for Calcium Efflux. Calcium-ion efflux from brain tissue does not appear to be a function of carrier frequency, since equivalent results are obtained at carrier frequencies of 50, 147, and 450 MHz provided the internal electric field intensity is the same in each brain. However, an important question remains why should there be alternate ranges, or windows, of internal electric field intensity which cause efflux enhancement An hypothesis that is consistent with and helps explain this finding is ... 

The specific carrier-wave amplitudes (field intensities) which have been found to be effective in producing Ca ion efflux are discussed in terms of tissue properties and relevant mechanisms. The brain tissue is hypothesized to be electrically nonlinear at specific field intensities this nonlinearity demodulates the carrier and releases a 16 Hz signal within ljie tissue. The 16 Hz signal is selectively coupled to the Ca ions by some mechanism, perhaps a dipolar-typ +(Maxwell-Wagner) relaxation, which enhances the efflux of Ca ions. The hypothesis that brain tissue exhibits a slight nonlinearity for certain values of applied RF electric field intensity is not testable by conventional measurements of e because changes... 

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