Potential, electrostatic oxidation

Use of idea on the role of electrostatic potential in oxide surface chemistry allows also to simulate the change in surface properties in clear way when various... 

When subjected to electrostatic attraction and thermal agitation, counterions form a diffuse layer in the solution, beyond the OHP. The electric potential caused by the surface charge and measured at the OHP (at the limit of the diffuse layer) is the zeta potential, <(, which is calculated from the electrophoretic mobility. This is the only mea.surable potential for oxide particles. The charge of the diffuse layer, uj, represents the countercharge of the particle (Figure 6.3). Since it compensates for the surface charge, electroneutrality imposes ao + cr = 0. 

As shown in Figure 2, adsorption of dispersants on particle surfaces can increase 2eta potential further, enhancing electrostatic repulsion. Increased repulsion between particles is evidenced by lower viscosity in concentrated slurries, or decreased settling rates in dilute suspensions. The effect of added dispersants on settling of (anhydrous) iron oxide particles is shown in Figure 3. 

A Schejter, I Aviram, T Goldkorn. The contribution of electrostatic factors to the oxidation-reduction potentials of c-type cytochi omes. In C Ho, ed. Electron Transport and Oxygen Utilization. New York Elsevier North-Holland, 1982, pp 95-109. 

Thiol (s), 652, 667-668 disulfides from, 668 electrostatic potential map of, 75 from alkyl halides, 667 hybridization of, 20 naming, 667 odor of, 667 oxidation of, 668 pKa of, 604... 

Morishima et al. [75, 76] have shown a remarkable effect of the polyelectrolyte surface potential on photoinduced ET in the laser photolysis of APh-x (8) and QPh-x (12) with viologens as electron acceptors. Decay profiles for the SPV (14) radical anion (SPV- ) generated by the photoinduced ET following a 347.1-nm laser excitation were monitored at 602 nm (Fig. 13) [75], For APh-9, the SPV- transient absorption persisted for several hundred microseconds after the laser pulse. The second-order rate constant (kb) for the back ET from SPV- to the oxidized Phen residue (Phen+) was estimated to be 8.7 x 107 M 1 s-1 for the APh-9-SPV system. For the monomer model system (AM(15)-SPV), on the other hand, kb was 2.8 x 109 M-1 s-1. This marked retardation of the back ET in the APh-9-SPV system is attributed to the electrostatic repulsion of SPV- by the electric field on the molecular surface of APh-9. The addition of NaCl decreases the electrostatic interaction. In fact, it increased the back ET rate. For example, at NaCl concentrations of 0.025 and 0.2 M, the value of kb increased to 2.5 x 108 and... 

Figure 18.6 Energetics of the ORR at the heme/Cu site of CcO the enzyme couples oxidation of ferroc3ftochrome c (standard potential about —250 mV all potentials are listed with respect to a normal hydrogen electrode) to reduction of O2 (standard potential at pH 7 800 mV). Of the 550 mV difference, only 100 mV is dissipated to drive the reaction 220 mV is expanded to translocate four protons from the basic matrix compartment to the acidic IMS (inter-membrane space). In addition 200 mV is converted into transmembrane electrostatic potential as ferroc3ftochrome is oxidized in the IMS, but the charge-compensating protons are taken from the matrix. The potentials are approximate.

Streitz FH, Mintmire JW (1994) Electrostatic potentials for metal-oxide surfaces and interfaces. Phys Rev B 50(16) 11996-12003... 

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