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Dielectric Shielding of Ionic Charges in Aqueous Solutions of Different Ionic Strength

✍ Scribed by Luigi Fabbrizzi; Piero Paoletti; Markus C. Zobrist; Gerold Schwarzenbach


Publisher
John Wiley and Sons
Year
1973
Tongue
German
Weight
505 KB
Volume
56
Category
Article
ISSN
0018-019X

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✦ Synopsis


Abstract

The thermodynamic functions of the proton transfer H~2~tn^2+^+tn → 2 Htn^+^ (tn = 1,3‐diaminopropane) have been determined in aqueous solutions containing different amounts of KCl (0.05 ⩽ μ ⩽ 3.01). The free energy (−ΔG) of the process decreases, whereas the enthalpy (‐ΔH) increases with μ. There is reason to believe that the reaction is entirely controlled by the Coulomb forces between the two protonic charges. The electrostatic energy involved can be described in terms of a model incorporating an effective dielectric constant εe, such that δε~e~/δμ and δ^2^ε~e~/δμδT are both positive. The polarisation of pure water is produced by orientation of hydrogen‐bonded dipole molecules H~2~O, whereas the electrolyte solution is polarised in addition by dislocation of the ions K^+^ and Cl^−^. Our results demonstrate that the former type of polarisation is much more temperature dependent than the latter.


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