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The Anodic Behavior of Silver in Concentrated Chloride Solutions

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Warianty tytułu
Języki publikacji
EN
Abstrakty
EN
The processes on the silver electrode during its anodic polarization in concentrated chloride solutions (1,5 - 5,0 M) are identified. The analysis of the potentiodynamic E-I relationships showed, that the anodic polarization depends on the concentration of Cl ions and runs through two steps (peaks A and B). The first step - peak A corresponds to: a/the irreversible electrode reaction involving the adsorption of the reaction product - AgCl in the solution, in which concentration of Cl was less than 2M and b/ the reversible electrode reaction involving the adsorption of the AgCl type species (n=3,4), when the concentration of Cl was more than 4 M. The second step - peak B corresponds to: a/the increase of the passive layer of AgCl showing high porosity and a low ohmic resistance - in the solution in which concentration of Cl was less than 2 M and b/the anodic process, which follows the dissolution-precipitation model, in which the electrochemical reaction of AgCl formation precedes the chemical precipitation of AgCl - in the solution with Cl was more than 4 M. On the basis of experimental functions the values of specific conductivity for the passive layer of AgCl at 4 M and 5 M chloride solutions were calculated. The structure differences of the passive AgCl layer forming in the chloride solutions have been shown by the microscope scanning analysis.
Rocznik
Strony
349--360
Opis fizyczny
Bibliogr. 17 poz., rys.
Twórcy
  • Institute of Inorganic Chemistry and Metallurgy of Rare Elements Technical University 50-370 Wrocław, Poland
Bibliografia
  • 1. Gilbert P.T., The Use of Silver-Silver Chloride Reference Electrodes in Dilute Solutions, in Electrode Processes, 1, 320, Butterworths (1961).
  • 2. Ives D.J.G. and Janz G.J., Reference Electrodes, Academic Press, (1961).
  • 3. Kanbera K., Takeda K., Yamanura Y. and Kondo S., Solid State Ionics, 40-41, 955 (1990).
  • 4. Takeda K., Prog. Batteries Sol. Cells, 8, 195 (1989).
  • 5. Fleischmann M., Robinson J. and Waser R., J. Electroanal. Chem., 117, 257 (1981).
  • 6. Fleischmann M. and Hill J.R., J. Electroanal. Chem., 146, 353 (1983).
  • 7. Birss V.J. and Smith C.K., Electrochim. Acta, 32,259 (1987).
  • 8. Burstein G.T. and Misra R.D.K., Electrochim. Acta, 28, 363 (1983).
  • 9. Katan T., Szpak S. and Bennion D.N., J. Electrochem. Soc., 121, 757 (1974).
  • 10. Caramazza C., Gazz. Chim. Ital., 90, 1839 (1960).
  • 11. Fritz J.J., J. Solution Chem., 14, 865 (1985).
  • 12. Seward T.M., Geochim. Cosmochim. Acta, 40, 1329 (1976).
  • 13. Laviron E., Bull. Soc. Chim. France, 5, 2252 (1968).
  • 14. Angerstein-Koztowska H. and Conway B.E., J. Electroanal. Chem., 95, 1 (1979).
  • 15. Devilliers D., Lantelme F. and Chemla M., Electrochim. Acta, 31, 1235 (1986).
  • 16. Calandra A.J., De Tacconi N.R., Pereiro R. and Arvia A.J., Electrochim. Acta, 19, 901 (1974).
  • 17. Ambrose J., Barradas R.G., Belinko K. and Shoesmith D.W., J. Colloid. Interface Sci., 47,441 (1974).
Typ dokumentu
Bibliografia
Identyfikator YADDA
bwmeta1.element.baztech-article-BUJ2-0011-0001
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