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Reverse diffusion

Other sulfur-containing compounds Pardo et al. [115] have studied electrochemical oxidation of 2-mercaptopyridine N-oxide on Hg electrodes in aqueous solutions. It has been found that anionic form of this compound was oxidized to yield a radical. At low concentration, oxidation was reversible and the radical was strongly adsorbed. At high concentrations, this process was accompanied by diffusive reversible oxidation. Reorientation of the adsorbed 2-mercaptopyridine N-oxide molecules on Hg electrodes in the presence of Triton X-100 has been studied... [Pg.976]

Figure 5 illustrates the mixed gas diffusion data for a pair of runs using 60% CH4/4OX N2 as the feed gas. Note that N adsorption is a maximum at about 10 seconds for ZBS-15 while CH4 adsorption continues even after 15 minutes. It is important to realize that since N2 diffusion reverses after 10 seconds, Q in... [Pg.224]

C. Reverse selective surface diffusion Reverse selective skin layer, n (1-5 R > n Highly porous ceramic or 1 carbon support 7600 pm OD... [Pg.358]

Nearly all electrochemistry handbooks, textbooks, and reviews cover the CV current-voltage relationship of diffusing, reversible mediators at a planar electrode surface (i.e., ferricyanide reduction). Kissinger and Heineman provide a more than adequate description of CV, and we prefer readers look to this reference as well as electrochemistry textbooks for detailed theory. CV experiments are conducted... [Pg.135]

Peak potentials and peak currents are useful diagnostic parameters to calculate in CV. In diffusing, reversible systems such as ferri/ferrocyanide, the straightforward relations in Table 5.2 can be used to extract estimates of formal potential, reversibility, and even diffusion coefficients. Understanding how to extract parameters from known electrochemical systems will help users identify trends in less well-known biofilm systems. [Pg.139]

Figure 6.63 Schematic of dry cathode-wet anode inlet flow that results in diffusion reversal process in electrolyte. The arrows represent the direction of diffusion flux, not the net mass flux. (Adapted from Ref. [11].)... Figure 6.63 Schematic of dry cathode-wet anode inlet flow that results in diffusion reversal process in electrolyte. The arrows represent the direction of diffusion flux, not the net mass flux. (Adapted from Ref. [11].)...
Researchers and engineers did a lot of works on the water transfer in membrane. Water transfer in membrane has two main aspects. First, because of electric drag effect, water passes through the electrolyte to the cathode with protons. Thus, electromigration of water is related with the current density and the number of proton hydration. Second, if the water content of the cathode side is high, the water diffusion reversely occurs from the cathode to the anode. The quantity of water is proportional to the diffusion coefficient and membrane concentration gradient. It is inversely proportional to the thickness of the film. Based on this, different dynamic models related with water transmission in film are established, for example, the model of Shen and Li [20], describing the water molar quantity produced as follows ... [Pg.559]

Similarly to the response at hydrodynamic electrodes, linear and cyclic potential sweeps for simple electrode reactions will yield steady-state voltammograms with forward and reverse scans retracing one another, provided the scan rate is slow enough to maintain the steady state [28, 35, 36, 37 and 38]. The limiting current will be detemiined by the slowest step in the overall process, but if the kinetics are fast, then the current will be under diffusion control and hence obey the above equation for a disc. The slope of the wave in the absence of IR drop will, once again, depend on the degree of reversibility of the electrode process. [Pg.1940]

The bipolar junction transistor (BIT) consists of tliree layers doped n-p-n or p-n-p tliat constitute tire emitter, base and collector, respectively. This stmcture can be considered as two back-to-back p-n junctions. Under nonnal operation, tire emitter-base junction is forward biased to inject minority carriers into tire base region. For example, tire n type emitter injects electrons into a p type base. The electrons in tire base, now minority carriers, diffuse tlirough tire base layer. The base-collector junction is reverse biased and its electric field sweeps tire carriers diffusing tlirough tlie base into tlie collector. The BIT operates by transport of minority carriers, but botli electrons and holes contribute to tlie overall current. [Pg.2891]

At very low concentrations of water, or in foods held below the free2ing point of water, physical conditions may be such that the available water may not be free to react. Under these conditions, the water may be physically immobi1i2ed as a glassy or plastic material or it may be bound to proteins (qv) and carbohydrates (qv). The water may diffuse with difficulty and thus may inhibit the diffusion of solutes. Changes in the stmcture of carbohydrates and proteins from amorphous to crystalline forms, or the reverse, that result from water migration or diffusion, may take place only very slowly. [Pg.457]

Nonporous Dense Membranes. Nonporous, dense membranes consist of a dense film through which permeants are transported by diffusion under the driving force of a pressure, concentration, or electrical potential gradient. The separation of various components of a solution is related directiy to their relative transport rate within the membrane, which is determined by their diffusivity and solubiUty ia the membrane material. An important property of nonporous, dense membranes is that even permeants of similar size may be separated when their concentration ia the membrane material (ie, their solubiUty) differs significantly. Most gas separation, pervaporation, and reverse osmosis membranes use dense membranes to perform the separation. However, these membranes usually have an asymmetric stmcture to improve the flux. [Pg.61]

Pulse radiolysis results (74) have led other workers to conclude that adsorbed OH radicals (surface trapped holes) are the principal oxidants, whereas free hydroxyl radicals probably play a minor role, if any. Because the OH radical reacts with HO2 at a diffusion controlled rate, the reverse reaction, that is desorption of OH to the solution, seems highly unlikely. The surface trapped hole, as defined by equation 18, accounts for most of the observations which had previously led to the suggestion of OH radical oxidation. The formation of H2O2 and the observations of hydroxylated intermediate products could all occur via... [Pg.405]


See other pages where Reverse diffusion is mentioned: [Pg.108]    [Pg.449]    [Pg.332]    [Pg.308]    [Pg.83]    [Pg.101]    [Pg.104]    [Pg.363]    [Pg.108]    [Pg.449]    [Pg.332]    [Pg.308]    [Pg.83]    [Pg.101]    [Pg.104]    [Pg.363]    [Pg.2591]    [Pg.2597]    [Pg.2829]    [Pg.2953]    [Pg.124]    [Pg.314]    [Pg.331]    [Pg.57]    [Pg.89]    [Pg.246]    [Pg.22]    [Pg.205]    [Pg.411]    [Pg.68]    [Pg.277]    [Pg.289]    [Pg.496]    [Pg.146]    [Pg.153]    [Pg.181]    [Pg.119]    [Pg.196]    [Pg.82]    [Pg.400]    [Pg.452]    [Pg.456]    [Pg.399]    [Pg.536]    [Pg.393]   
See also in sourсe #XX -- [ Pg.49 ]

See also in sourсe #XX -- [ Pg.101 ]




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Reversible diffusion-controlled reactions

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