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Current electronic/ionic

Most of the models available in the literature are axial symmetric. A second simplification refers to the discretization adopted for the electrodes and electrolyte. Some of the models consider the cathode, electrolyte and anode as a whole and adopt an axial discretization. Electronic/ionic resistivity is computed as the average value of the single resistivites, calculated at the local temperature (Campanari and Iora, 2004). Using this approach means to simplify the solution of mass transfer in the porous media and the conservation of current. Authors have shown that about 200 elements are sufficient to describe the behaviour of a cell 1.5 m long using a finite volume approach (Campanari and Iora, 2004). [Pg.213]

Chazalviel et proposed a model that differs from Lehmann s only in the cause of the phase transformation. Their model is based on a defective nature of the oxide and the change of oxide property is considaed to be due to a sudden loss in the ion and electron blocking properties of the oxide. Breakdown of oxide occurs at the high field condition resulting in a large electronic current or ionic current. [Pg.213]

To explore further the significance of the electrical conductivity results, we need to discuss briefly the nature of electric currents. An electric current can travel along a metal wire because electrons are free to move through the wire the moving electrons carry the current. In ionic substances, the ions carry the current. Therefore, substances that contain ions can conduct an electric current only if the ions can move—the current travels by the movement of the charged ions. In solid NaCl, the ions are tightly held and cannot move. When the solid melts and becomes a liquid, however, the structure is disrupted and the ions can move. As a result, an electric current can travel through the melted salt. [Pg.81]

In order for a substance to conduct electricity, it must possess charged particles that can move (in a metal, mobile electrons can carry the electric current). Solid ionic compounds do not conduct electricity - the ions are held firmly by strong electrostatic forces and cannot move. When the substance is melted or dissolved in water, however, the ions move freely and can carry an electric current. An aqueous solution, or melt, of an ionic substance that behaves in this way, is called an electrolyte. [Pg.51]

Membrane Electronic/Ionic Phase Feed Oxygen Rate Current [O2I mA/cm [cc/min-cm l Thickness mm... [Pg.95]

An electrolyte is a substance with ionic DC conductivity. Intracellular and extracellular liquids contain ions free to migrate. In pure electroljrtes, the charge carriers are ions, and there is no separate flow of electrons—they are all bound to their respective atoms. Therefore, tissue DC currents are ionic currents, in contrast to the electronic current in metals. This is not contradictory to a possible local electronic conductance due to free electrons (e.g., in the intracellular DNA molecules). New solid materials such as organic polymers and glasses may contain an appreciable amount of free ions with considerable mobility therefore, the materials of an electrolytic measuring cell are not limited to liquid media. Some of these solid media show a mixture of ionic and electronic conductivity. [Pg.9]

Key components of any fuel cell are the anode and cathode catalyst layers (CLs). One of the layers converts the electron current into ionic current, and the other performs the reverse conversion. The dependence of voltage loss (overpotential) in the electrode on current is of primary interest for any application. [Pg.648]

In this configuration, the current is passed from one element to the next via the current collector, and is collected at the battery s terminal plates. This considerably reduces the battery s internal resistance and ensures homogenous distribution of the current (electronic and ionic). These characteristics mean this architecture is a natural choice for the optimization of systems functioning with a strong current. [Pg.253]

When an external potential difference is applied to the cell, the electronic current through the oxide is normally no longer equal to the ionic current electrons can be produced at the electrodes. The oxidation rate can thus be influenced by changing the externally applied potential difference. In principle, the oxidation process can be completely stopped by applying a counter potential difference numerically equal to the driving force of the oxidation reaction ... [Pg.574]

Figure 82. Depiction of the Differential Aeration Hypothesis (DAH) for localized corrosion showing the coupling currents (electronic through the metal, ionic through the solution) from the corrosion cavity to the external surface, where the two currents annihilate via a charge transfer reaction involving a cathodic depolarizer (e.g., reduction of oxygen). Reprinted from Corrosion Science, 32 (1991) 51, Copyright (1991), with permission from NACE International... Figure 82. Depiction of the Differential Aeration Hypothesis (DAH) for localized corrosion showing the coupling currents (electronic through the metal, ionic through the solution) from the corrosion cavity to the external surface, where the two currents annihilate via a charge transfer reaction involving a cathodic depolarizer (e.g., reduction of oxygen). Reprinted from Corrosion Science, 32 (1991) 51, Copyright (1991), with permission from NACE International...
Electronic resistance is almost negligible, even when graphite or graphite/polymer composites are used as current collectors. Ionic and... [Pg.44]

Key characteristics of selected hydrocarbon oxidation electrodes Direct Oxidation Catalysts Reforming Catalysts Cracking catalysts Current Collection Mixed Electronic/Ionic Conductors Electrochemical enhancement... [Pg.177]

Fast ionic conductors are used as solid electrolytes in fuel cells and sensors. The search for fast ion conductors operating near room temperature is a matter of current electronic materials research. The practical small-scale application of some types of fuel cells as replacements for batteries may hinge on success in this search. [Pg.46]

At low currents, the rate of change of die electrode potential with current is associated with the limiting rate of electron transfer across the phase boundary between the electronically conducting electrode and the ionically conducting solution, and is temied the electron transfer overpotential. The electron transfer rate at a given overpotential has been found to depend on the nature of the species participating in the reaction, and the properties of the electrolyte and the electrode itself (such as, for example, the chemical nature of the metal). [Pg.603]

Figure 16.1 Simple dry cell battery. Electrons are conducted along the external circuit (4), which physically connects the active (2) and noble (1) materials. An equivalent ionic counter-current is conducted through the electrolyte (3), thereby completing the circuit. Figure 16.1 Simple dry cell battery. Electrons are conducted along the external circuit (4), which physically connects the active (2) and noble (1) materials. An equivalent ionic counter-current is conducted through the electrolyte (3), thereby completing the circuit.

See other pages where Current electronic/ionic is mentioned: [Pg.530]    [Pg.58]    [Pg.571]    [Pg.415]    [Pg.101]    [Pg.111]    [Pg.309]    [Pg.119]    [Pg.145]    [Pg.181]    [Pg.102]    [Pg.58]    [Pg.462]    [Pg.92]    [Pg.530]    [Pg.1656]    [Pg.108]    [Pg.66]    [Pg.612]    [Pg.275]    [Pg.664]    [Pg.158]    [Pg.111]    [Pg.127]    [Pg.206]    [Pg.2751]    [Pg.2927]    [Pg.42]    [Pg.429]    [Pg.331]    [Pg.526]    [Pg.362]    [Pg.49]    [Pg.175]    [Pg.362]   
See also in sourсe #XX -- [ Pg.9 ]




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