Big Chemical Encyclopedia

Chemical substances, components, reactions, process design ...

Articles Figures Tables About

Coupling, kinetic potential

The two-dimensional, coupled kinetic and transport model can also be used to simulate start-stop processes. Figure 14 plots cathode potential and carbon corrosion current distribution at three instants when the H2/02 front passes through 10, 50, and 90% of anode flow path during the start process. As H2 displaces air in the anode flow-field, the size of the power source increases and the load size decreases accordingly. The balanced current density becomes larger, causing higher carbon corrosion current density. [Pg.72]

Maurits, N.M., Fraaije, J.G.E.M. Mesoscopic dynamics of copolymer melts from density dynamics to external potential dynamics using nonlocal kinetic coupling. J. Chem. Phys. 107 (1997) 5879-5889. [Pg.36]

Figure 7-15. Healing and equilibration phase of a typical MD simulation, In the ideal case, the temperature should fluctuate around the desired value (here 298 K), and the potential energy should remain constant. Remember that the total energy is the sum of potential and kinetic energy, the latter being directly coupled to the temperature of the system,... Figure 7-15. Healing and equilibration phase of a typical MD simulation, In the ideal case, the temperature should fluctuate around the desired value (here 298 K), and the potential energy should remain constant. Remember that the total energy is the sum of potential and kinetic energy, the latter being directly coupled to the temperature of the system,...
If the initial concentration of Cu + is 1.00 X 10 M, for example, then the cathode s potential must be more negative than -1-0.105 V versus the SHE (-0.139 V versus the SCE) to achieve a quantitative reduction of Cu + to Cu. Note that at this potential H3O+ is not reduced to H2, maintaining a 100% current efficiency. Many of the published procedures for the controlled-potential coulometric analysis of Cu + call for potentials that are more negative than that shown for the reduction of H3O+ in Figure 11.21. Such potentials can be used, however, because the slow kinetics for reducing H3O+ results in a significant overpotential that shifts the potential of the H3O+/H2 redox couple to more negative potentials. [Pg.497]


See other pages where Coupling, kinetic potential is mentioned: [Pg.474]    [Pg.126]    [Pg.58]    [Pg.123]    [Pg.1364]    [Pg.229]    [Pg.82]    [Pg.169]    [Pg.287]    [Pg.2121]    [Pg.422]    [Pg.579]    [Pg.65]    [Pg.1027]    [Pg.1800]    [Pg.2462]    [Pg.2731]    [Pg.2732]    [Pg.2]    [Pg.4]    [Pg.221]    [Pg.387]    [Pg.400]    [Pg.509]    [Pg.511]    [Pg.768]    [Pg.7]    [Pg.338]    [Pg.367]    [Pg.370]    [Pg.403]    [Pg.167]    [Pg.433]    [Pg.408]    [Pg.367]    [Pg.277]    [Pg.54]    [Pg.179]    [Pg.274]    [Pg.477]    [Pg.707]    [Pg.853]    [Pg.182]    [Pg.214]    [Pg.217]    [Pg.766]   
See also in sourсe #XX -- [ Pg.137 ]




SEARCH



Kinetic coupling

Kinetic potential

© 2024 chempedia.info