The adsorption of M-naphthalenesulfonate, B-naphthalenesulfonate and 1, 5-naphthalenedisulfonate ions on mercury from an aqueous solution at constant ionic strength has been investigated by measurement of the double layer capacity as a function of concentration. The adsorption can be represented by
Specific adsorption of acetate ions at the mercury—lithium acetate (AQ) interface
✍ Scribed by M.V. Ramanamurti; B.V. Apparao
- Publisher
- Elsevier Science
- Year
- 1978
- Tongue
- English
- Weight
- 482 KB
- Volume
- 23
- Category
- Article
- ISSN
- 0013-4686
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✦ Synopsis
Specific adsorption of acetate ions at the mercury-lithium acetate (aq) interface has been investigated using both differential capacity and electrocapillary measurements. Variation of charge due to snrface excess of lithium ions (q+) and of charge due to specifically adsorbed acetate ions (q-l) with electrode charge (qH) have been discussed. Such discussion inferred superequivalent adsorption of acetate ions at all positive charges for concentrations of lithium acetate 20.20 M whereas Bin-Markov plots predicted the absence of specific adsorptidn; the prediction of Esin-Markov plots has been shown to be faulty under certain conditions. The plots of #I"-'us 4-l at constant qM for acetate ion resembled the corresponding plots for F-and BF; ions: the slope of these plots is negative up to coverages corresponding to 0.20 M lithium acetate. The identification of the isotherm parameter, (a+"-2/&-')p~ with the reciprocal of inner layer capacity at constant charge d-,C') has been questioned
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