The adsorption bhaviour of &PO; anions on mercury has previously been analysed from capacitance-potential relations at the interface of mercury with K&PO,. It is not possible to determine unambiguously the adsorption characteristics of I&PO, ions from siagle salt solution experiments because of the
The adsorption of formate and acetate ions on mercury electrodes from constant ionic strength solutions
β Scribed by Ernesto R. Gonzalez; Artur J. Motheo
- Publisher
- Elsevier Science
- Year
- 1989
- Tongue
- English
- Weight
- 538 KB
- Volume
- 34
- Category
- Article
- ISSN
- 0013-4686
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β¦ Synopsis
The adsorption of formate and acetate ions on mercury electrodes was studied at 25Β°C from constant ionic strength solutions of composition XM HCQQNa+(O.S-x) M NaF and rcM CH,CQQNa + (0.5 -K) M NaF, respectively. The adsorption characteristics of the two anions are compared with previous results in single salt solutions. In both cases, the adsorbed charges are low and the characteristics of the inner layer suggest that the anions are adsorbed with the participation of the solvent. A virial isotherm with a second virial coefficient of 0.7 nm2/ion was found to describe adequately the behaviour of both anions.
π SIMILAR VOLUMES
The adsorption of Br-anions has been studied from propylene carbonate solutions of low ionic strength (0.16 h4) at mercury. A maximum on the capacity curve is observed at low Br-ion concentration, a result which is unusual for strongly adsorbed ions. A new method of analysing the interfacial thermod
The adsorption of lead (11) from chloride-bromide mixtures of a high ionic strength (I=4 mol/L) to mercury electrodes was studied using square wave voltammetry, differential, and normal pulse polarography. The presence of excess chloride ions in the solution prevents additional surface complexation