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In theoretical chemistry, Specific ion Interaction Theory (SIT theory) is a theory used to estimate single-ion activity coefficients in electrolyte solutions at relatively high concentrations. [ 1 ] [ 2 ] It does so by taking into consideration interaction coefficients between the various ions present in solution.
This theory was very successful for dilute solutions of 1:1 electrolytes and, as discussed below, the Debye–Hückel expressions are still valid at sufficiently low concentrations. The values calculated with Debye–Hückel theory diverge more and more from observed values as the concentrations and/or ionic charges increases.
The molar ionic strength, I, of a solution is a function of the concentration of all ions present in that solution. [3]= = where one half is because we are including both cations and anions, c i is the molar concentration of ion i (M, mol/L), z i is the charge number of that ion, and the sum is taken over all ions in the solution.
Electrolyte balance is maintained by oral, or in emergencies, intravenous (IV) intake of electrolyte-containing substances, and is regulated by hormones, in general with the kidneys flushing out excess levels. In humans, electrolyte homeostasis is regulated by hormones such as antidiuretic hormones, aldosterone and parathyroid hormones.
m is known as the limiting molar conductivity, K is an empirical constant, and c is the electrolyte concentration. ("Limiting" here means "at the limit of the infinite dilution".) In effect, the observed conductivity of a strong electrolyte becomes directly proportional to concentration at sufficiently low concentrations, i.e. when
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Going towards high dilutions good results have been found using liquid membrane cells, it has been possible to investigate aqueous media 10 −4 M and it has been found that for 1:1 electrolytes (as NaCl or KCl) the Debye–Hückel equation is totally correct, but for 2:2 or 3:2 electrolytes it is possible to find negative deviation from the ...
The Ostwald law of dilution provides a satisfactory description of the concentration dependence of the conductivity of weak electrolytes like CH 3 COOH and NH 4 OH. [3] [4] The variation of molar conductivity is essentially due to the incomplete dissociation of weak electrolytes into ions.