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Reaction cell, electrochemical

For the electrochemical cell reaction, the reaction free energy AG is the utilizable electrical energy. The reaction enthalpy AH is the theoretical available energy, which is increased or reduced by an amount TAS. The product of the temperature and the entropy describes the amount of heat consumed or released reversibly during the reaction. With tabulated values for the enthalpy and the entropy it is possible to obtain AG. ... [Pg.10]

Equation (5) shows the fundamental relationship between Gibbs free energy change of the chemical reaction and the cell potential under reversible conditions (potential of the electrochemical cell reaction). [Pg.6]

Figure 9 illustrates the results for kg. Neither the volume of activation for diffusion AVdiff (average —0.9 l.lcm mol ) nor the electrochemical cell reaction volumes A VAg/AgCl average (—22 2 cm mol i) for the C0W12 couple show significant dependence on electrolyte identity or concentration. For the PWi2 / ... [Pg.631]

An electrochemical cell reaction, like any oxidation-reduction reaction, can be written as the sum of an oxidation half-reaction and a reduction half-reaction. In the case of a cell, these half-reactions correspond to the reactions at the two electrodes. Since the cell reaction is the sum of the half-cell reactions, it is convenient to think of dividing the cell potential into half-cell potentials. Unfortunately, there is no way of measuring a half-cell potential—we always need two half-cells to make a cell, the potential of which is measurable. By convention, the half-cell reaction,... [Pg.172]

Finally, when it comes to electricity cost, electro-organic reactions do not have to be driven backward many desired products can be obtained by electrochemical cell reactions that have negative AG s. If these reactions can be broken up into two reactions in an electrochemical cell, they form a kind of fuel cell that is intrinsically electrogenerative, so now electricity is being made and can be used elsewhere—the electricity costs have turned into a gain (Section 13.3). [Pg.89]

Nernst equation — A fundamental equation in -> electrochemistry derived by - Nernst at the end of the nineteenth century assuming an osmotic equilibrium between the metal and solution phases (- Nernst equilibrium). This equation describes the dependence of the equilibrium electrode - potential on the composition of the contacting phases. The Nernst equation can be derived from the - potential of the cell reaction (Ecen = AG/nF) where AG is the - Gibbs energy change of the - cell reaction, n is the charge number of the electrochemical cell reaction, and F is the - Faraday constant. [Pg.444]

Determine the entropy and enthalpy change of an electrochemical cell reaction. [Pg.450]

This overall electrochemical cell reaction is equivalent to transporting the Na COg phase physically from one side of the substrate to the other. [Pg.124]

It is useful to establish a more generalized representation for the electrochemical cell reaction as follows ... [Pg.37]

The constant potential amperometric detector determines the current generated by the oxidation or reduction of electoactive species at a constant potential in an electrochemical cell. Reactions occur at an electrode surface and proceed by electron transfer to or from the electrode surface. The majority of electroactive compounds exhibit some degree of aromaticity or conjugation with most practical applications involving oxidation reactions. Electronic resonance in aromatic compounds functions to stabilize free radical intermediate products of anodic oxidations, and as a consequence, the activation barrier for electrochemical reaction is lowered significantly. Typical applications are the detection of phenols (e.g. antioxidants, opiates, catechols, estrogens, quinones) aromatic amines (e.g. aminophenols, neuroactive alkaloids [quinine, cocaine, morphine], neurotransmitters [epinephrine, acetylcoline]), thiols and disulfides, amino acids and peptides, nitroaromatics and pharmaceutical compounds [170,171]. Detection limits are usually in the nanomolar to micromolar range or 0.25 to 25 ng / ml. [Pg.479]

An electrochemical cell reaction (overall reaction) includes at least two halfcell reactions or electrode reactions that either liberate or consume electrons. For the overall reaction (2), for example, the halfcell reactions might be expressed as ... [Pg.10]

If this is a reversible electrochemical cell reaction, we have as previously mentioned ... [Pg.19]

Corrosion by gases occurs with chemical reactions between metals and gases, which produces two effects on the metal (1) metal is consumed, and (2) metal properties are changed. Although corrosion by gases is similar to corrosion by liquids, two important differences are found. First, in gases, the products of corrosion usually remain on the surface, forming in some systems a protective film second, local electrochemical cell reactions are suppressed. [Pg.530]


See other pages where Reaction cell, electrochemical is mentioned: [Pg.168]    [Pg.625]    [Pg.827]    [Pg.355]    [Pg.50]    [Pg.611]    [Pg.123]    [Pg.227]    [Pg.289]    [Pg.384]    [Pg.58]    [Pg.58]    [Pg.59]    [Pg.157]    [Pg.11]    [Pg.2140]    [Pg.270]    [Pg.631]    [Pg.66]    [Pg.141]    [Pg.38]    [Pg.2126]    [Pg.62]    [Pg.62]    [Pg.62]    [Pg.62]    [Pg.77]    [Pg.77]    [Pg.10]    [Pg.2]    [Pg.147]    [Pg.375]    [Pg.634]   
See also in sourсe #XX -- [ Pg.367 ]




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Electrochemical Reactions in Fuel Cells

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Half-reactions electrochemical cells

Half-reactions in electrochemical cells

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