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Kwak JC, Joshi YM. The binding of divalent metal ions to polyelectrolytes in mixed counterion systems. I. The dye spectrophotometric method. Biophys Chem. 1981;13(1):55-64doi: 10.1016/0301-4622(81)80025-7.
Kwak, J. C., & Joshi, Y. M. (1981). The binding of divalent metal ions to polyelectrolytes in mixed counterion systems. I. The dye spectrophotometric method. Biophysical chemistry, 13(1), 55-64. https://doi.org/10.1016/0301-4622(81)80025-7
Kwak, J C, and Joshi, Y M. "The binding of divalent metal ions to polyelectrolytes in mixed counterion systems. I. The dye spectrophotometric method." Biophysical chemistry vol. 13,1 (1981): 55-64. doi: https://doi.org/10.1016/0301-4622(81)80025-7
Kwak JC, Joshi YM. The binding of divalent metal ions to polyelectrolytes in mixed counterion systems. I. The dye spectrophotometric method. Biophys Chem. 1981 Feb;13(1):55-64. doi: 10.1016/0301-4622(81)80025-7. PMID: 17000159.
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Biophys Chem. 1981 Feb;13(1):55-64. doi: 10.1016/0301-4622(81)80025-7.

The binding of divalent metal ions to polyelectrolytes in mixed counterion systems. I. The dye spectrophotometric method.

Biophysical chemistry

J C Kwak, Y M Joshi

Affiliations

  1. Department of Chemistry, Dalhousie University, Halifax, Nova Scotia, Canada B3H 4J3.

PMID: 17000159 DOI: 10.1016/0301-4622(81)80025-7

Abstract

The dye spectrophotometric method for the measurement of the activity of divalent metal ions in polyelectrolyte solutions containing added electrolytes is discussed. The method is applied to mixtures containing the dextransulfate polyanion, NaCl, and MgCl2 or Ca2. A two wavelength ratio method as applied to polyelectrolyte solutions is compared to the standard method which makes use of the previous determination of the dye-metal ion formation constant. The ratio method is found to be a convenient and reliable method which is not influenced by decomposition of the dye or by statistical errors in the extrapolation procedure. The activity coefficients as determined by the two wavelength dye spectrophotometric method are compared to results of Donnan exclusion measurements, and of EMF measurements using a calcium ion selective electrode. The results of the spectrophotometric method are equal to those of the two other methods within the limits of error in the latter. The spectrophotometric measurements can extend to much lower ion activaties than the other two methods, and can be done in the presence of a large excess of added electrolyte, yielding results of considerably improved precision when compared to Donnan and EMF methods.

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