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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 ...
According to Gauss’s law, a conductor at equilibrium carrying an applied current has no charge on its interior.Instead, the entirety of the charge of the conductor resides on the surface, and can be expressed by the equation: = where E is the electric field caused by the charge on the conductor and is the permittivity of the free space.
Smoluchowski's sedimentation potential is defined where ε 0 is the permitivity of free space, D the dimensionless dielectric constant, ξ the zeta potential, g the acceleration due to gravity, Φ the particle volume fraction, ρ the particle density, ρ o the medium density, λ the specific volume conductivity, and η the viscosity.
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
In 1923, Peter Debye and Erich Hückel reported the first successful theory for the distribution of charges in ionic solutions. [7] The framework of linearized Debye–Hückel theory subsequently was applied to colloidal dispersions by S. Levine and G. P. Dube [8] [9] who found that charged colloidal particles should experience a strong medium-range repulsion and a weaker long-range attraction.
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 ...
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
The following figure employs the linearized equation and the high potential graphing equation derived above. It is a potential-versus-distance graph for varying surface potentials of 50, 100, 150, and 200 mV. The equations employed in this figure assume an 80mM NaCl solution. Potential versus distance for varying surface potentials of 50, 100 ...