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The zeta potential is an important and readily measurable indicator of the stability of colloidal dispersions. The magnitude of the zeta potential indicates the degree of electrostatic repulsion between adjacent, similarly charged particles in a dispersion. For molecules and particles that are small enough, a high zeta potential will confer ...
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The zeta function can be thought of as the determinant of the resolvent. The zeta function plays an important role in studying dynamical systems. Note that this is the same general type of zeta function as the Riemann zeta function; however, in this case, the corresponding kernel is not
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. [8]
where ε r is the dielectric constant of the dispersion medium, ε 0 is the permittivity of free space (C 2 N −1 m −2), η is dynamic viscosity of the dispersion medium (Pa s), and ζ is zeta potential (i.e., the electrokinetic potential of the slipping plane in the double layer, units mV or V).
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 ...
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