Big Chemical Encyclopedia

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

Articles Figures Tables About

Galvanic cells spontaneity

There are two principal methods of applying cathodic protection, viz. the impressed current technique and the use of sacrificial anodes. The former includes the structure as part of a driven electrochemical cell and the latter includes the structure as part of a spontaneous galvanic cell. [Pg.115]

When a solid electrolyte component is interfaced with two electronically conducting (e.g. metal) films (electrodes) a solid electrolyte galvanic cell is formed (Fig. 3.3). Cells of this type with YSZ solid electrolyte are used as oxygen sensors.8 The potential difference U R that develops spontaneously between the two electrodes (W and R designate working and reference electrode, respectively) is given by ... [Pg.94]

In a galvanic cell, a spontaneous chemical reaction draws electrons into the cell through the cathode, the site of reduction, and releases them at the anode, the site of oxidation. [Pg.612]

Secondary cells are galvanic cells that must be charged before they can be used this type of cell is normally rechargeable. The batteries used in portable computers and automobiles are secondary cells. In the charging process, an external source of electricity reverses the spontaneous cell reaction and creates a nonequilibrium mixture of reactants. After charging, the cell can again produce electricity. [Pg.638]

C19-0015. The thermite reaction between aluminum metal and iron oxide is so rapid and exothermic that it generates a fountain of sparks (see photo) and can melt the container in which it takes place. The spontaneity of this reaction suggests the possibility of a galvanic cell involving aluminum and... [Pg.1377]

C19-0016. Use tabulated thermodynamic data to verily that the galvanic cell of Section Exercise is spontaneous in the direction written. [Pg.1378]

Electrons always flow spontaneously downhill from higher electrical potential to lower electrical potential. In a galvanic cell, the electrode with the higher potential is designated by convention as the negative electrode. The electrode with the lower potential is designated as the positive electrode. [Pg.1381]

A galvanic cell can be constmcted from a zinc electrode immersed in a solution of zinc sulfate and an iron electrode immersed in a solution of iron(II) sulfate. What is the standard potential of this cell, and what is its spontaneous direction under standard conditions ... [Pg.1386]

The standard potential for any galvanic cell is determined by subtracting the more negative standard reduction potential from the more positive standard reduction potential. A positive E ° indicates spontaneity under standard conditions. [Pg.1388]

In a galvanic cell, a spontaneous chemical reaction generates an electrical current. It is also possible to use an electrical current to drive a nonspontaneous chemical reaction. The recharging of a dead battery uses an external electrical current to drive the batteiy reaction in the reverse, or uphill, direction. [Pg.1408]

Two directions of current flow in galvanic cells are possible a spontaneous direction and an imposed direction. When the cell circuit is closed with the aid of electronic conductors, current will flow from the cell s positive electrode to its negative electrode in the external part of the circuit, and from the negative to the positive electrode within the cell (Fig. 2.2a). In this case the current arises from the cell s own voltage, and the cell acts as a chemical source of electric current or battery. But when a power source of higher voltage, connected so as to oppose the cell, is present in the external circuit, it will cause current to flow in the opposite direction (Fig. 2.2b), and the cell works as an electrolyzer. [Pg.32]

Having introduced matters pertaining to the electrochemical series earlier, it is only relevant that an appraisal is given on some of its applications. The coverage hereunder describes different examples which include aspects of spontaneity of a galvanic cell reaction, feasibility of different species for reaction, criterion of choice of electrodes to form galvanic cells, sacrificial protection, cementation, concentration and tempera lure effects on emf of electrochemical cells, clues on chemical reaction, caution notes on the use of electrochemical series, and finally determination of equilibrium constants and solubility products. [Pg.650]

Internal electrolysis is the term applied by Sand1,2 to an electrogravimetric analysis proceeding spontaneously without the application of an external voltage, i.e., by the short-circuited galvanic cell. [Pg.24]

Potentiometry deals with the electromotive force (EMF) generated in a galvanic cell where a spontaneous chemical reaction is taking place. In practice, potentiometry employs the EMF response of a galvanostatic cell that is based on the measurement of an electrochemical cell potential under zero-current conditions to determine the concentration of analytes in measuring samples. Because an electrode potential generated on the metal electrode surface,... [Pg.628]

When using the Nernst equation on a cell reaction in which the overall reaction is not supplied, only the half-reactions and concentrations, there are two equivalent methods to work the problem. The first way is to write the overall redox reaction based upon E° values and then apply the Nernst equation. If the Ecell turns out to be negative, it indicates that the reaction is not a spontaneous one (an electrolytic cell) or that the reaction is written backwards if it is supposed to be a galvanic cell. If it is supposed to be a galvanic cell, then all you need to... [Pg.272]

A galvanic cell is one in which this current flows (and the redox reaction proceeds) spontaneously because of the strong tendency for the chemical species involved to give and take electrons. An electrolytic cell is one in which the current is not a spontaneous current, but rather is the result of incorporating an external power source, such as a battery, in the circuit to drive the reaction in one direction or the other. Potentiometric methods involve galvanic cells, and voltammetric and amperometric methods involve electrolytic cells. [Pg.393]

A cell is a complete electroanalytical system consisting of an electrode at which reduction occurs, as well as an electrode at which oxidation occurs, and including the connections between the two. A half-cell is half of a cell in the sense that it is one of the two electrodes (and associated chemistry) in the system, termed either the reduction half-cell or the oxidation half-cell. The anode is the electrode at which oxidation takes place. The cathode is the electrode at which reduction takes place. An electrolytic cell is one in which the current that flows is not spontaneous, but rather due to the presence of an external power source. A galvanic cell is a cell in which the current that flows is spontaneous. [Pg.540]

A galvanic cell operates of its own accord as a result of a spontaneous redox reaction. An electrolytic cell operates as a result of an external power source (e.g., a battery) in the circuit. [Pg.540]

You know that galvanic cells have positive standard cell potentials, and that these cells use spontaneous chemical reactions to produce electricity. You also know that electrolytic cells have negative standard cell potentials, and that these cells use electricity to perform non-spontaneous chemical reactions. Thus, you can use the sign of the standard cell potential to predict whether a reaction is spontaneous or not under standard conditions. [Pg.534]

In this section, you learned about electrolytic cells, which convert electrical energy into chemical energy. You compared the spontaneous reactions in galvanic cells, which have positive cell potentials, with the non-spontaneous reactions in electrolytic cells, which have negative cell potentials. You then considered cells that act as both galvanic cells and electrolytic cells in some common rechargeable batteries. These batteries are an important application of electrochemistry. In the next two sections, you will learn about many more electrochemical applications. [Pg.537]

The galvanic cell pictured in Figure 7.1 is not at equilibrium. If switch S is closed, electrons will spontaneously flow from the zinc (anode) to the copper (cathode) electrode. This flow will continue imtil the reactants and products attain their equilibrium concentrations. If switch S is opened before the cell reaches equilibrium, the electron flow will be interrupted. The voltmeter would register a positive voltage, which is a measure of the degree to which the redox reaction drives electrons from the anode to the cathode. Since this voltage is a type of energy that has the potential to do work, it is referred to as a redox potential or cell potential, denoted as... [Pg.174]

Tabulated E values can be used to calculate the for any reaction, as illustrated in Table 7.2 for the Zn/Cu galvanic cell. The redox reaction is spontaneous when the half-reaction (Cu /Cu) with the larger reduction (+0.34V) acts as the oxidizing agent. In this case, the other half-reaction (Zn /Zn) proceeds as an oxidation. The halfcell potential for this reduction is +0.76 V as it represents the reverse of the half-cell reduction potential as listed in Table 7.2. The sum of the oxidation and reduction half reactions is +0.34V + 0.76 V = +1.10 V. Thus for the galvanic Zn/Cu cell is +1.10V. [Pg.176]

Galvanic cell A device in which chemical energy from a spontaneous redox reaction is changed to electrical energy that can be utilized for power. [Pg.191]

A galvanic cell uses a spontaneous chemical reaction to generate electricity. [Pg.274]


See other pages where Galvanic cells spontaneity is mentioned: [Pg.240]    [Pg.240]    [Pg.841]    [Pg.610]    [Pg.611]    [Pg.630]    [Pg.1408]    [Pg.1408]    [Pg.581]    [Pg.668]    [Pg.670]    [Pg.265]    [Pg.320]    [Pg.250]    [Pg.509]    [Pg.524]    [Pg.535]    [Pg.230]    [Pg.173]    [Pg.180]    [Pg.88]    [Pg.400]    [Pg.274]    [Pg.291]    [Pg.692]    [Pg.18]    [Pg.26]   
See also in sourсe #XX -- [ Pg.831 ]




SEARCH



Cell galvanics

© 2024 chempedia.info