Kenrick's method has been used to obtain real free energies of soivation '"A%, of H+ and Clin water-ethanol and water-DMF solutions. The difference of the surface potentials bXHSo -x\*) has been determined by the extrapolation of the differences of the real free energies of solvation of ions in wate
Shift of the scale of potentials, changes of the surface potential on the solution/air interface, change of the potential on the solution/mercury interface and of the liquid junctions potentials for water-isopropanol mixtures
โ Scribed by J. Jakuszewski; M. Przasnyski; H. Scholl; A. Siekowska
- Publisher
- Elsevier Science
- Year
- 1975
- Tongue
- English
- Weight
- 363 KB
- Volume
- 20
- Category
- Article
- ISSN
- 0013-4686
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โฆ Synopsis
We
have measured the potentials of zero charge of mercury in water-iso-propanol mixtures and the changes of real free energy of solvation of hydrogen ion in these mixtures. With the help of extrapolation of functions obtained from above measurements from the potential of the reference electrode we have determined the shift of the standard potentials scale ('A"p":, ), differences of the surface potentials ('A"x), difference of the liquid junctions potentials ("A-4,) and values of the potentials effects ("A-g,, J produced by the exchange of the solvent's molecules on the surface of mercury at potential of zero charge for system water-iso-propanol.
We have also proposed a new method for determinmg values 'A,,, 'Aw&, "A"g,i,, basing on the assumption that one of the values "Awpy, to be determined shows rapld changes at small additions of water while changes of the other values appear mainly at small contents of a nonaqueous component m a mixture.
๐ SIMILAR VOLUMES
The zero-charge potentials of gallium in water as determined from the position of the minimum on the differential capacitance in dilute solutions and from the electrocapillary curves in the absence of anion adsorption are shown to coincide and to be -@97 to -0.98 V (nce). Evidence is presented supp