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Densities and Apparent Molar Volumes of Aqueous Solutions of K4Fe(CN)6, K3Fe(CN)6, K3Co(CN)6, K2Ni(CN)4, and KAg(CN)2 at 293 to 343 K
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Densities and Apparent Molar Volumes of Aqueous Solutions of K4Fe(CN)6, K3Fe(CN)6, K3Co(CN)6, K2Ni(CN)4, and KAg(CN)2 at 293 to 343 K

L. Hnědkovský, Y. Kianinia and G. Hefter
Journal of Chemical & Engineering Data, Vol.63(10), pp.3860-3873
2018
DOI: https://doi.org/10.1021/acs.jced.8b00513
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Abstract

Densities of aqueous solutions of K4Fe(CN)6, K3Fe(CN)6, K3Co(CN)6, K2Ni(CN)4, and KAg(CN)2 have been measured with a vibrating-tube densimeter at temperatures from 293.15 to 343.15 at 5 K intervals over the approximate concentration range 0.02 to 0.4 mol·kg–1. Apparent molar volumes, Vϕ, calculated from these data were fitted with an extended form of the Redlich–Rosenfeld–Meyer equation to obtain the standard partial molar quantities, V°. The Vϕ and V° values for all the salts are in reasonable agreement with literature data at all temperatures. Deviations of the Vϕ values from the Debye–Hückel limiting law were found to increase considerably with increasing anion charge. Values of V° for the cyanometallate anions were obtained using an appropriate extrathermodynamic assumption and were found to increase with increasing crystallographic size or ionic charge except for Fe(CN)64–, which shows a remarkable contraction of more than 35 cm3·mol–1 relative to Fe(CN)63–. The origins of this anomaly are unclear. Isobaric expansivities, α, of all the salt solutions show the greatest increase with solute concentration, but the smallest dependence on the nature of the anion, at lower temperatures. These effects are consistent with the dissolved ions changing from water-structure breaking to net structure making with increasing temperature.

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Citation topics
2 Chemistry
2.89 Ionic, Molecular & Complex Liquids
2.89.462 Excess Molar Volumes
Web Of Science research areas
Chemistry, Multidisciplinary
Engineering, Chemical
Thermodynamics
ESI research areas
Chemistry
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