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Dispersion charge

According to the Scher-MontroU model, the dispersive current transient (Fig. 5b) can be analyzed in a double-log plot of log(i) vs log(/). The slope should be —(1 — ct) for t < and —(1 + a) for t > with a sum of the two slopes equal to 2, as shown in Figure 5c. For many years the Scher-MontroU model has been the standard model to use in analyzing dispersive charge transport in polymers. [Pg.411]

The quaternary methylated diammines (CH3)3N(CH2)pN(CH3)3+ could be obtained from a methanol-water solution also for lower p values, i.e. p > 2. The greater stability of these doubly charged ions can be attributed to the more dispersed charge and to the absence of protic hydrogens. [Pg.288]

Arkhipov VI, lovu MS, Rudenko AI, Shutov SD (1979) Analysis of the dispersive charge transport in vitreous 0.55 AS2S3-O.45 86283. Physica Status Solidi (a) 54 67... [Pg.60]

CI,C is less basic than F,C . F can disperse charge only by an inductive effect [see Fig. 3-5( )j. In addition to an inductive effect. Cl uses its empty 3d orbitals to disperse charge by p-d tr bonding, see Fig. 3-5(fc). F is a second-period element with no 2d orbitals. [Pg.42]

Sw2-reactions of charge types 1, 3, and 4 (see p. 171) all have more highly dispersed charge in the transition state than in the ground state. The effect on... [Pg.177]

Figure 2.4.4 (A) Time-dependent electric current generated from the oxidation of HTC coal in an indirect carbon fuel cell. Solutions of Fe 111 and Vv were prepared in 0.5 mol L 1 H2SO4. (B) Development of open-circuit potential Eoc (up) and current I (down) due to Fe2+ formation in the anodic half-cell via oxidation of HTC coal, indicating the reducing potential of bare hydrothermal carbon (HC) dispersions. Charge equalization between the two half-cells was assured by a salt bridge containing a saturated KC1 solution. Carbon felt was used as electrodes. (C) Comparison of hydrothermal and fossil carbon sources in the same setup. Figure 2.4.4 (A) Time-dependent electric current generated from the oxidation of HTC coal in an indirect carbon fuel cell. Solutions of Fe 111 and Vv were prepared in 0.5 mol L 1 H2SO4. (B) Development of open-circuit potential Eoc (up) and current I (down) due to Fe2+ formation in the anodic half-cell via oxidation of HTC coal, indicating the reducing potential of bare hydrothermal carbon (HC) dispersions. Charge equalization between the two half-cells was assured by a salt bridge containing a saturated KC1 solution. Carbon felt was used as electrodes. (C) Comparison of hydrothermal and fossil carbon sources in the same setup.
Exchange repulsion Dispersion Charge transfer Charge-charge Dipole-dipole Polarization of i by j... [Pg.87]

Polycatenar compounds, with more than one terminal chain at each end of a rod-like molecule can also exhibit columnar phases, although they possess a linear molecular structure. Three linear molecules aggregate together to form a self-assembled disc. These discs then stack up to form a fluid columnar structure. Non-dispersive charge-carrier mobility in such polycatenar compounds has also been found. ... [Pg.162]

How both the density and mobility of charge carriers in metals and band semiconductors (i.e. those in which electrons are not localized by disorder or correlation) are influenced by particular features of the electronic structure, namely band dispersion and band Ailing, will now be examined. Taking mobUity first, this book will briefly revisit the topic of band dispersion. Charge carriers in narrow bands have a lower mobility because they... [Pg.258]

Now, some addition reactions will be considered, the solvent dependences of which have been reviewed [77, 78]. Addition of uncharged electrophiles [e.g. Br2, ArS—Cl, NO—Cl, R—CO3H) to carbon-carbon multiple bonds leads to the development of a small, usually dispersed charge in the activated complex. In more polar solvents, this is accompanied by a slight rate acceleration. In reactions with substantial charge development in the activated complex, larger rate accelerations with increasing solvent polarity are observed. [Pg.176]

Hartwich, G., Lossau, H., Michel-Beyerle, M. E., and Ogrodnik, A., 1998, Nonexponential fluorescence decay in reaction centers of Rhodobacter sphaeroides reflecting dispersive charge separation up to 1 ns. J. Phys. Chem., 102 3815n3820. [Pg.669]

Dicker G, de Haas MP, Warman JM, de Leeuw DM, Siebbeles LDA. (2004) The disperse charge-carrier kinetics in regioregular poly(3-hexylthiophene). JPhys Chem B 108 17818-17824. [Pg.198]

G releases electrons disperses charge stabilizes cation... [Pg.163]

Leong, Y.K., Interparticle forces arising from an adsorbed strong polyelectrolyte in colloidal dispersions Charged patch attraction. Colloid Polym. Sci., 277, 299, 1999. [Pg.1011]


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See also in sourсe #XX -- [ Pg.148 ]

See also in sourсe #XX -- [ Pg.67 , Pg.70 , Pg.71 ]




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Charge dispersive

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