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                                Voltaic Cells in Electrochemistry and Surface Chemistry of Liquids
                                cording to their data, the value of γ * γ* over wide ranges of HCl
                                                               1
                                                                   2
                                                               i / i
                                concentrations  does  not  depend  upon  the  presence  of  surface-active  sub-
                                stances (e.g., n-heptyl and n-nonyl alcohols) in the experiments.
                                       VIII.  REAL POTENTIALS OF IONS IN SOLID
                                                     ELECTROLYTES
                                The possibility of measuring the Volta potential in the system metal–solid-
                                state electrolyte and using the data obtained to determine ionic compo-
                                nents of the free lattice energy has been shown in our papers. 67–68  Earlier,
                                                69
                                Copeland and Seifert  measured the Volta potential between Ag and solid
                                                                             o
                                AgNø  3  in the temperature range between 190 and 280  C.=They investi-
                                gated  the  potential jump  during  the  phase  transition  from  solid  to  liquid
                                salt.
                                                                      M
                                    Our measurements of the Volta potentials, ∆ MX Ψ,in systems Ag–AgX
                                                      - -
                                                   -
                                and Cd–CdX (for X=Cl ,Br ,I ) were performed using voltaic cells; see
                                Fig. 7 for an Ag–AgX  system.=
                                    Applying  the  condenser  or  ionization  methods  (Section  IV),= the
                                voltage  E is  determined  as  the  difference  in  the  compensating  voltages
                                                                 Ag
                                                     E = E –  =∆ Agx Ψ                 (13)
                                                         5 E6
                                of the  following two  cells:




















                                                Figure 7.  The differences of real poten-
                                                        +
                                                tials of the Ag  ion in metal-solid electro-
                                                lyte systems.=
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