ISSN:
0001-1541
Keywords:
Chemistry
;
Chemical Engineering
Source:
Wiley InterScience Backfile Collection 1832-2000
Topics:
Chemistry and Pharmacology
,
Process Engineering, Biotechnology, Nutrition Technology
Notes:
This study forms part of a project aimed at obtaining a better understanding of the behavior of nonideal permselective membranes. The object here was to determine the applicability of the Nernst-Planck equations for studying the behavior of ions in aqueous solutions surrounding such a membrane during electrodialysis.Attention was confined to stagnant and laminar flow systems. The processes studied were transfer of hydrogen ions, silver ions, and mixtures of the two through the cation exchanging membrane Nepton CR-61. The bulk solution concentrations on either side of the membrane varied from 0.01 to 0.20 N, and in all cases the only anions present were nitrate ions. Limiting currents for solutions of silver nitrate were predictable within 15%, with much of the uncertainty resulting from the difficulty in defining the limiting current. For mixtures of silver nitrate and nitric acid the limiting currents were predictable within the range of experimental accuracy but were found to be quite sensitive to small changes in the operating conditions. This sensitivity results from the very high relative mobility of the hydrogen ions. The relative transport of the two cations was primarily a function of relative concentration, relative diffusivities, current density, and ion exchange equilibria and was predictable with an accuracy limited only by the uncertainty of the ionic diffusivities and the ion exchange equilibria.The diffusivities of the cations in the membrane relative to the diffusivity of nitrate ion were estimated to be about ten times lower than in solution. This was explained by assuming that the cations tended to concentrate about the anionic fixed charges of the membrane thereby portially screening their effectiveness and reducing the mobility of the cations. In mixtures, the membrane diffusivity of the silver ions relative to the hydrogen ions was lower (by a factor of 1.4 to 3.6) than the relative diffusivity in solution. This indicated that silver ions were more easily concentrated about the fixed charges and thereby screened them from both the anions and hydrogen ions.
Additional Material:
10 Ill.
Type of Medium:
Electronic Resource
URL:
http://dx.doi.org/10.1002/aic.690080120
