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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.
Total ionic strength adjustment buffer (TISAB) is a buffer solution which increases the ionic strength of a solution to a relatively high level. This is important for potentiometric measurements, including ion selective electrodes, because they measure the activity of the analyte rather than its concentration.
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 ...
The strength of the M-O bond tends to increase with the charge and decrease as the size of the metal ion increases. In fact there is a very good linear correlation between hydration enthalpy and the ratio of charge squared to ionic radius, z 2 /r. [4] For ions in solution Shannon's "effective ionic radius" is the measure most often used. [5]
where z is the electrical charge on the ion, I is the ionic strength, ε and b are interaction coefficients and m and c are concentrations. The summation extends over the other ions present in solution, which includes the ions produced by the background electrolyte. The first term in these expressions comes from Debye–Hückel theory.
The polyelectrolyte film thickness is dependent upon its ionic strength. [13] charged species on polyelectrolyte chains repel each other, causing the chains to stretch out. As the salt concentration increases, ionic strength increases, and the ions will shield the charges on the polymer chain allowing the polymer chain to form a dense random ...
The extended Debye–Hückel equation provides accurate results for μ ≤ 0.1. For solutions of greater ionic strengths, the Pitzer equations should be used. In these solutions the activity coefficient may actually increase with ionic strength. The Debye–Hückel plot with different values for ion charge Z and ion diameter a
The relationship between the solubility of a protein and increasing ionic strength of the solution can be represented by the Cohn equation: = S = solubility of the protein, B is idealized solubility, K is a salt-specific constant and I is the ionic strength of the solution, which is attributed to the added salt.