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Batteries Nernst equation

This is useful, albeit basic, information for an ES working in the domain of sick cars. If you are employed as a car mechanic, you are not likely to benefit from, or even be interested in, the presence within the knowledge base of details about how lead sulfate batteries degrade with age and how any diminution in concentration of the active materials in the battery can be related through the Nernst equation to a reduction in its voltage. In the context of car repair, all that you need to know is that the battery is dead and the car will not start, so it will need replacing or recharging. [Pg.212]

Tower, Stephen. All About Electrochemistry. Available online. URL http //www.cheml.com/acad/webtext/elchem/. Accessed May 28, 2009. Part of a virtual chemistry textbook, this excellent resource explains the basics of electrochemistry, which is important in understanding how fuel cells work. Discussions include galvanic cells and electrodes, cell potentials and thermodynamics, the Nernst equation and its applications, batteries and fuel cells, electrochemical corrosion, and electrolytic cells and electrolysis. [Pg.162]

Equations (8.55), (8.57) make it easy to see the connection between cell potential and reaction spontaneity. When is positive (AG < 0), the cell reaction is spontaneous, allowing useful electrical work to be withdrawn (i.e., the battery is draining ). Conversely, when is negative (AG > 0), the cell reaction is spontaneous, requiring input work from the surroundings (i.e., the battery is charging ). When = 0 (AG = 0), the cell reaction is at equilibrium, and, in accordance with (8.27d), the Nernst equation reduces to... [Pg.294]

Because conditions under which a battery is operating (such as temperature and concentration of reactants) can change, different potentials can be reached. The new electrode potential, E, can be calculated using the Nernst equation ... [Pg.162]

Nernst equation An equation that correlates chemical energy and the electric potential of a galvanic cell or battery. Links the actual reversible potential of an electrode (measured in volts), E, at nonstandard conditions of concentration or pressure, to the standard reversible potential of the electrode couple, EO, which is a thermodynamic value. The Nernst equation is named after the German physical chemist Walther Nernst. [Pg.192]

Tb see why a nicad battery produces a constant voltage, write the Nernst equation for its reaction. Look at Q. [Pg.889]

Ni(OH)2 and NiOOH coexist in a single phase of a homogenous solid-state solution, and their relative concentration ratio in the solid solution varies with the state of charge (SOC) of the cell. Therefore, the cathode potential varies with the battery SOC governed by the Nernst equation. The temperature coefficient of the cathode reaction is about —0.5mV/°C. [Pg.1898]

Nernst equation (13.3) nickel-cadmium battery (13.5) nickel-metal-hydride battery (13.5) oxidation (13.2) oxidation-reduction (13.2) passivation (corrosion) (13.8)... [Pg.568]

The decrease in free energy of the system in a spontaneous redox reaction is equal to the electrical work done by the system on the surroundings, or AG = nFE. The equilibrium constant for a redox reaction can be found from the standard electromotive force of a cell. 10. The Nernst equation gives the relationship between the cell emf and the concentrations of the reactants and products under non-standard-state conditions. Batteries, which consist of one or more galvanic cells, are used widely as self-contained power sources. Some of the better-known batteries are the dry cell, such as the Leclanche cell, the mercury battery, and the lead storage battery used in automobiles. Fuel cells produce electrical energy from a continuous supply of reactants. [Pg.873]

The Great Nernst Hiatus." In direct potentiometry using membrane electrodes, a similar situation has occurred in the past 8 decades. Every quantitative and instrumental analysis textbook has treated the glass electrode as a battery obeying the principles of reversible thermodynamics and the Nernst equation. [Pg.289]

Nernst equation (20.7) zinc-carbon (Leclanche) dry cell (20.8) alkaline dry cell (20.8) lithium-iodine battery (20.8) lead storage cell (20.8) nickel-cadmium cell (20.8)... [Pg.843]

The Nernst equation provides the operating principle for batteries, electrolysis (the production of hydrogen and oxygen gases from w ater), electroplating, oxidations and reductions, and corrosion. These processes all depend on the equilibrium between a charged solid surface and its corresponding ions in solution. [Pg.412]

The dependence of the equilibrium voltage on the concentration of dissolved components is given by the Nernst equation (Eq. (8)), and reads for the lead-acid battery as an example ... [Pg.35]

Actually, Ion analyzer, as a high input impedance millivoltmeter, is widely used in measuring the EMF of the battery which is composed by ion selective electrode, reference electrode, and solution. The concentration of the unknown solution is acquired through measuring the EMF margin between standard solution and tested solution under the same electrode system. By the Nernst equation the authors have inferred... [Pg.12]

During his Leipzig period, Nernst performed a series of electrochemical studies from which, at the age of twenty-five, he arrived at his well-known equations. These equations described the concentration dependence of the potential difference of galvanic cells, such as batteries, and were of both great theoretical and practical importance. Nernst started with the investigation of the diffusion of electrolytes in one solution. Then he turned to the diffusion at the boundary between two solutions with different electrolyte concentrations he determined that the osmotic pressure difference would result in an electric potential difference or electromotive force (emf). Next he divided both solutions into two concentration half-cells, connected to each other by a liquid junction, and measured the emf via electrodes dipped into both solutions. The data supported his first equation where the... [Pg.830]

No attempt has been made so far to relate the membrane phctse concentration of an ion to its external concentration. A relation of the type (3.3.120e, f) may be derived by using the relation (3.3.118b) for Donnan equilibrium as well as the electroneutrality relations in the membrane and in the external solution. The ionic flux of any ion through an ion exchange membrane may then be obtained from the Nernst-Plank equation (3.1.106). If is to be eliminated from such an equation, then the following procedure may be adopted. Write down the flux for /J and /j. If there is some constraint like Jl 0 (as in (3.4.121)), the problem is easily solved. In some cases, /J = (for example, in battery separators for alkaline Ni/Zn batteries, KOH is the electrolyte and/k+ = /oh-)- This will also allow elimination of V(i. Then one can express / in terms of the concentrations of two solutions on the two sides of the membrane by integrating across the battery separator membrane at steady state. [Pg.189]

When the membrane potential is the same as the Nernst potential for a particular type of ions, the ion current due to these ions is zero, if all kinds of ions were to behave independently of each other. This situation corresponds to the equilibrium condition discussed in Section 8.2. When Vm differs from the Nernst potential, there is a net current. The result of Equation 8.39 can be conveniently represented as an equivalent electrieal circuit. Consider a resistor of resistance Ri = 1/gi and a battery of the Nernst potential Vi placed in series between the in and out terminals (Figure 8.3a). Since the resistor and the battery are in series, the current h and the voltage difference between the in terminal and the out terminal are related as... [Pg.217]

Figure 8>3 Electrical equivalent circuits for a pore, (a) The Nernst battery of potential V and a resistor of resistance R-, are in series. The voltage difference between the in and out terminals is the sum of the voltage drops from the resistor and the Nernst battery (Equation 8.41). (b) The charged membrane acts like a capacitor in parallel to the arrangement in (a). Figure 8>3 Electrical equivalent circuits for a pore, (a) The Nernst battery of potential V and a resistor of resistance R-, are in series. The voltage difference between the in and out terminals is the sum of the voltage drops from the resistor and the Nernst battery (Equation 8.41). (b) The charged membrane acts like a capacitor in parallel to the arrangement in (a).

See other pages where Batteries Nernst equation is mentioned: [Pg.226]    [Pg.89]    [Pg.225]    [Pg.396]    [Pg.111]    [Pg.1089]    [Pg.1130]    [Pg.2609]    [Pg.226]    [Pg.289]    [Pg.300]    [Pg.818]    [Pg.48]    [Pg.225]    [Pg.283]    [Pg.137]    [Pg.232]    [Pg.350]    [Pg.380]    [Pg.364]   
See also in sourсe #XX -- [ Pg.651 ]




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