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Counteracting diffusion potential

The degree of diffusion between small and large droplets will be reduced because the presence of Z2 means that a counteracting concentration potential is more rapidly established. [Pg.400]

The greater sensitivity of differential pulse polarography can be attributed to two sources an enhancement of the faradaic current or a decrease in the non-faradaic charging current. To account for the enhancement, consider the events that must occur in the surface layer around an electrode as the potential is suddenly increased by 50 mV. If a reactive species is present in this layer, there will be a surge of current that lowers the reactant concentration to that demanded by the new potential. As the equilibrium concentration for that potential is approached, however, the current decays to a level just sufficient to counteract diffusion (that is, to the diffusion-controlled current). In classical polarography, the initial surge of cur-... [Pg.690]

Theoretically, at a low Uappl the counteraction would be expected to result in full polarization of the electrodes, i.e., would become equal to Eappl, so no current will be passed however, the actual pc,2 at the electrode surface is continuously diminished by diffusion of the Cl2 gas into the solution and so there results a residual current, i = (2 appl - E fR. The amount of the latter increases more or less gradually with increasing Uappl, because the actual pC 2 increases until it finally becomes 1 atm, where Cl2 gas starts to escape from the solution. In the meantime, the anode has been completely covered with Zn metal, so that [Zn] has become unity. In fact, E has now attained a constant maximum value, the so-called decomposition potential, where electrolysis really breaks through. Any further increase in app) would, according to first expectations, cause a linear current increase, i = ( app, - Edecomp )IR. However, Fig. 3.2 shows that the experimental current curve deviates more and... [Pg.115]

In a qualitative way, colloids are stable when they are electrically charged (we will not consider here the stability of hydrophilic colloids - gelatine, starch, proteins, macromolecules, biocolloids - where stability may be enhanced by steric arrangements and the affinity of organic functional groups to water). In a physical model of colloid stability particle repulsion due to electrostatic interaction is counteracted by attraction due to van der Waal interaction. The repulsion energy depends on the surface potential and its decrease in the diffuse part of the double layer the decay of the potential with distance is a function of the ionic strength (Fig. 3.2c and Fig. [Pg.251]

The most significant effect of a convective-diffusive transport mechanism is to counteract the tendency of the electronation-current density to reduce the interfacial concentration of electron acceptors to zero. Further, since the interfacial concentration of electron acceptors then remains at a value above that given by the diffusion-based equations, a transition time, indicated by a rapid potential variation, need not be attained. [Pg.512]

This model is based on the Gouy-Chapman theory (diffuse double-layer theory). The theory states that in the area of the boundary layer between solid and aqueous phase, independently of the surface charge, increased concentrations of cations and anions within a diffuse layer exists because of electrostatic forces. In contrast to the constant-capacitance model, the electrical potential does not change up to a certain distance from the phase boundaries and is not immediately declining in a linear manner (Fig. 14 a). Diffusion counteracts these forces, leading to dilution with increasing distance from the boundary. This relation can be described physically by the Poisson-Boltzmann equation. [Pg.33]

Unfortunately, the use of the terms osmotic pressure and osmotic potential, as well as their algebraic sign, varies in the literature. Osmotic pressures have been measured using an osmometer (Fig. 2-8), a device having a membrane that ideally is permeable to water but not to the solutes present. When pure water is placed on one side of the membrane and some solution on the other, a net diffusion of water occurs toward the side with the solutes. To counteract this tendency and establish equilibrium, a hydrostatic pressure is necessary on the solution side. This pressure is often called the osmotic... [Pg.65]

Although Spheramine s effect in the brain is locally restricted due to its small diffusion diameter, the dose of 325 000 cells to be administered bilaterally (650000 cells total per patient) represents a small Junctional dose increase per body side as a small effect to the homolateral side must be expected. This small functional dose increase is considered safe because all patients will continue to take oral anti-PD medication and a sufficient buffer of oral dopaminergics that can be reduced to counteract potential overdosing is warranted. [Pg.355]

The end of the presynaptic cell contains small vesicles, spherical collections of the same lipid molecules that make up the cell membrane. Inside these vesicles, neurotransmitters exist in high concentrations. When the action potential reaches the end of the presynaptic cell, some of the vesicles merge with the cell membrane and release their contents (a process called exocytosis). The released neurotransmitters experience an immediate concentration gradient. They diffuse away from the release point to counteract the gradient, and in doing this, they cross the synapse and arrive at the neighboring cell. [Pg.833]

In practice, the excess oleic or aqueous phase usually emulsifies into the conjugate microemulsion phase upon agitation. The reason is that the surfactant-rich continuous microemulsion phase resists coalescence of the surfactant-poor excess phase, presumably because surfactant depletion in the thinning microemulsion phase is counteracted by surfactant diffusion to restore uniform chemical potential (Gibbs Marangoni stability). In addition, macroemulsions formed from three-phase microemulsion systems tend to... [Pg.587]


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See also in sourсe #XX -- [ Pg.216 ]




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