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Activity coefficient
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==== Ion trios ==== The rise in activity coefficients found with most aqueous strong electrolyte systems can be explained by increasing electrostatic repulsions between ions of the same charge which are forced together as the available space between them decreases. In this way, the initial attractions between cations and anions at the low concentrations described by Debye and Hueckel are progressively overcome. It has been proposed<ref>{{Cite journal |last=May |first=Peter M. |last2=May |first2=Eric |date=2024 |title=Ion Trios: Cause of Ion Specific Interactions in Aqueous Solutions and Path to a Better pH Definition |url=https://pubs.acs.org/doi/10.1021/acsomega.4c07525 |journal=ACS Omega |volume=9 |issue=46 |pages=46373β46386 |doi=10.1021/acsomega.4c07525|pmc=11579776 }}</ref> that these electrostatic repulsions take place predominantly through the formation of so-called ion trios in which two ions of like charge interact, on average and at distance, with the same counterion as well as with each other. This model accurately reproduces the experimental patterns of activity and osmotic coefficients exhibited by numerous 3-ion aqueous electrolyte mixtures.
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