COULOSTATIC STUDY OF ADSORPTION KINETICS AT A METAL-ELECTROLYTE INTERFACE. I. THEORY

Abstract

Variations of the surface concentration and ptotential with time are derived for the coulostatic method for an adsorption process obeying the logarithmic Temkin isotherm at equilibrium at an ideal polarized electrode and for mixed control by semi-infinite linear diffusion and adsorption kinetics. It is assumed that the charge density on the electrode varies according to a step-function of time in such a way that the cell with the ideal polarized electrode is essentially at open circuit after the abrupt change of charge density. Limiting cases corresponding to pure control by either adsorption kinetics or diffusion are also considered. The evaluation of the adsorption exchange rate from potential-time variations is indicated. A coulostatic method was suggested for the study of adsorption kinetics of a neutral substance at a metal-electrolyte interface. The influence of mass transfer control was not considered. The more general case with control by adsorption kinetics and mass transfer, as determined by semi-infinite linear diffusion, i analyzed here. (Author)

Document Details

Document Type
Technical Report
Publication Date
May 01, 1962
Accession Number
AD0283681

Entities

People

  • Paul Delahay

Organizations

  • Louisiana State University

Tags

Communities of Interest

  • Materials and Manufacturing Processes

DTIC Thesaurus Topics

  • Adsorption
  • Charge Density
  • Diffusion
  • Electrodes
  • Electrolytes
  • Isotherms
  • Kinetics
  • Mass Transfer
  • Step Functions
  • Test And Evaluation

Readers

  • Combustion science or combustion engineering.
  • Electrochemical Surface Science
  • Structural Dynamics.