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  2. Ionic strength - Wikipedia

    en.wikipedia.org/wiki/Ionic_strength

    The ionic strength of a solution is a measure of the concentration of ions in that solution. Ionic compounds , when dissolved in water, dissociate into ions. The total electrolyte concentration in solution will affect important properties such as the dissociation constant or the solubility of different salts .

  3. Potentiator - Wikipedia

    en.wikipedia.org/wiki/Potentiator

    Low ionic strength saline (LISS) is a potentiator that acts by not only reducing the zeta potential, but also by increasing the amount of antibody taken up by the red blood cell during sensitization. LISS is a solution of glycine and albumin. Polyethylene glycol (PEG) in a LISS solution removes water from the system and thus concentrates the ...

  4. Thermodynamic activity - Wikipedia

    en.wikipedia.org/wiki/Thermodynamic_activity

    Although at low ionic strength (< 0.1 M) the activity coefficient approaches unity, this coefficient can actually increase with ionic strength in a high ionic strength regime. For hydrochloric acid solutions, the minimum is around 0.4 M. [3]

  5. Pitzer equations - Wikipedia

    en.wikipedia.org/wiki/Pitzer_equations

    Expressions were derived for the variation of single-ion activity coefficients as a function of ionic strength. 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.

  6. Inert salt - Wikipedia

    en.wikipedia.org/wiki/Inert_salt

    The real goal is to reduce changes in the activity coefficients of ionic species which allows the definition of conditional equilibrium or rate constants. Any salt will affect the ionic strength, inert salts have the additional property that both the cations and the anions of the salt do or should not not interfere in any way with the molecules ...

  7. Debye–Hückel theory - Wikipedia

    en.wikipedia.org/wiki/Debye–Hückel_theory

    For very low values of the ionic strength the value of the denominator in the expression above becomes nearly equal to one. In this situation the mean activity coefficient is proportional to the square root of the ionic strength. This is known as the Debye–Hückel limiting law. In this limit the equation is given as follows [14]: section 2.5.2

  8. Polyelectrolyte adsorption - Wikipedia

    en.wikipedia.org/wiki/Polyelectrolyte_adsorption

    In a low ionic strength solution, the charges present on the repeat units of the polymer are the dominant force controlling conformation. Since there is very little charge present to screen the repulsive interactions between the repeat units, the polymer assumes a very spread out, loose conformation.

  9. Common-ion effect - Wikipedia

    en.wikipedia.org/wiki/Common-ion_effect

    In chemistry, the common-ion effect refers to the decrease in solubility of an ionic precipitate by the addition to the solution of a soluble compound with an ion in common with the precipitate. [1] This behaviour is a consequence of Le Chatelier's principle for the equilibrium reaction of the ionic association / dissociation .