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Ionic Product and Enthalpy of Ionization of Water from Electromotive Force Measurements

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dc.contributor.author Covington, Arthur K
dc.contributor.author Ferra, M. Isabel A
dc.contributor.author Robinson, Robert A
dc.date.accessioned 2025-12-27T05:43:58Z
dc.date.available 2025-12-27T05:43:58Z
dc.date.issued 1977
dc.identifier.uri http://dspace.bits-pilani.ac.in:8080/jspui/handle/123456789/20457
dc.description.abstract New e.m.f. data have been obtained for the cell: Pt, H2|MOH,NX|AgX|Ag at 25°C where M, N = Li, Na, K, Cs and X = Cl, Br, from which the ionic product (Kw) of water can be obtained (pKw= 14.004). Application of a theory of mixed electrolyte solutions to the results enables the variation of the apparent ionic product (K′w) with ionic strength and cation to be expressed in terms of the properties of the pure alkali metal halide and hydroxide solutions at the same total ionic strength. The conditions M = Li, N = K, X = Cl were selected for a study over the temperature range 0–60°C and from these measurements the enthalpy of ionization of water was calculated (ΔH°= 13430 ± 5 cal mol–1). The use of mixed cations in the cell minimises the variation of apparent ionic product with ionic strength, thereby reducing the uncertainty in the extrapolation to zero ionic strength felt previously to be the principal contributing factor leading to the discrepancy between calorimetric and e.m.f. derived values for the ionization enthalpy of water. en_US
dc.language.iso en en_US
dc.publisher Journal of the Chemical Society : Faraday Transaction - I. The Chemical Society, London. 1977, 73 (11) en_US
dc.subject Chemistry en_US
dc.subject Enthalpy of ionization en_US
dc.subject Thermodynamic properties en_US
dc.subject Journal of the Chemical Society : Faraday Transaction - I en_US
dc.title Ionic Product and Enthalpy of Ionization of Water from Electromotive Force Measurements en_US
dc.type Thesis en_US


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