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Zeta potential titration is a titration of heterogeneous systems, for example colloids and emulsions. Solids in such systems have very high surface area. This type of titration is used to study the zeta potential of these surfaces under different conditions. Details of zeta potential definition and measuring techniques can be found in the ...
In other words, zeta potential is the potential difference between the dispersion medium and the stationary layer of fluid attached to the dispersed particle. The zeta potential is caused by the net electrical charge contained within the region bounded by the slipping plane, and also depends on the location of that plane. Thus, it is widely ...
The potential of zero charge is used for determination of the absolute electrode potential in a given electrolyte. IUPAC also defines the potential difference with respect to the potential of zero charge as: E pzc = E − E σ=0. where: E pzc is the electrode potential difference with respect to the point of zero charge, E σ=0
Electrokinetic phenomena generally measure zeta potential, and a zero zeta potential is interpreted as the point of zero net charge at the shear plane. This is termed the isoelectric point. [29] Thus, the isoelectric point is the value of pH at which the colloidal particle remains stationary in an electrical field.
Zeta potential titration This page was last edited on 30 March 2013, at 12:34 (UTC). Text is available under the Creative Commons Attribution-ShareAlike ...
For example, from Fe 2+ + 2 e − ⇌ Fe(s) (–0.44 V), the energy to form one neutral atom of Fe(s) from one Fe 2+ ion and two electrons is 2 × 0.44 eV = 0.88 eV, or 84 907 J/(mol e −). That value is also the standard formation energy (∆ G f °) for an Fe 2+ ion, since e − and Fe( s ) both have zero formation energy.
Potentiometry passively measures the potential of a solution between two electrodes, affecting the solution very little in the process. One electrode is called the reference electrode and has a constant potential, while the other one is an indicator electrode whose potential changes with the sample's composition. Therefore, the difference in ...
In number theory, the local zeta function Z(V, s) (sometimes called the congruent zeta function or the Hasse–Weil zeta function) is defined as (,) = (= ())where V is a non-singular n-dimensional projective algebraic variety over the field F q with q elements and N k is the number of points of V defined over the finite field extension F q k of F q.