Strong electrolytes reference states

The equilibrium constant for reaction (89), based on nole-fraction-composltion, strong-electrolyte standard states fOr HC1[I 0] and DGl[DoO]. is 0-715 at 298.I5 K. Because this value of K for reaction C89) refers to strong electrolytes,we can rewrite equation (89) as... 

Solutions of electrolytes form a class of thermodynamic systems for which the concept of species is all-important. In this section we discuss the problems of reference and standard states for strong electrolytes as solutes dissolved in some solvent. 

These equations are used whenever we need an expression for the chemical potential of a strong electrolyte in solution. We have based the development only on a binary system. The equations are exactly the same when several strong electrolytes are present as solutes. In such cases the chemical potential of a given solute is a function of the molalities of all solutes through the mean activity coefficients. In general the reference state is defined as the solution in which the molality of all solutes is infinitesimally small. In special cases a mixed solvent consisting of the pure solvent and one or more solutes at a fixed molality may be used. The reference state in such cases is the infinitely dilute solution of all solutes except those whose concentrations are kept constant. Again, when two or more substances, pure or mixed, may be considered as solvents, a choice of solvent must be made and clearly stated. 

NaCI is present in solution as ions. Compounds that are completely ionized in water are called strong electrolytes because these solutions easily conduct electricity. Most salts are strong electrolytes. Other compounds (including many acids and bases) may dissolve in water without completely ionizing. These are referred to as weak electrolytes and their state of ionization is at equilibrium with the larger molecule. Those compounds that dissolve with no ionization (e.g., glucose, C6H12O6) are called nonelectrolytes. 

Relationships analogous to those given above may be derived in an exactb similar manner for the activities referred to mole fractions or molarities. As seen in 37c, the activities for the various standard states, based on the ideal dilute solution, can be related to one another by equation (37.7). The result is, however, applicable to a single molecular species the corresponding relationships between the mean ionic activity coefficients of a strong electrolyte, assumed to be completely ionized, are found to be... 

The main purpose of this contribution, however, is to review recent advances in solid state ionics achieved by means of microelectrodes, i.e. electrodes whose size is in the micrometer range (typically 1-250 pm). In liquid electrolytes (ultra)-microelectrodes are rather common and applied for several reasons they exhibit a very fast response in voltametric studies, facilitate the investigation of fast charge transfer reactions and strongly reduce the importance of ohmic drops in the electrolyte, thus allowing e.g. measurements in low-conductive electrolytes [33, 34], Microelectrodes are also employed to localize reactions on electrodes and to scan electrochemical properties of electrode surfaces (scanning electrochemical microscope [35, 36]) further developments refer to arrays of microelectrodes, e.g. for (partly spatially resolved) electroanalysis [37-39], applications in bioelectrochemistry and medicine [40, 41] or spatially resolved pH measurements [42], Reviews on these and other applications of microelectrodes are, for example, given in Ref. [33, 34, 43-47],... 

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