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The term colloidal suspension refers unambiguously to the overall mixture (although a narrower sense of the word suspension is distinguished from colloids by larger particle size). A colloid has a dispersed phase (the suspended particles) and a continuous phase (the medium of suspension).
Surface charge emits an electric field, which causes particle repulsion and attraction, affecting many colloidal properties. [2] Surface charge practically always appears on the particle surface when it is placed into a fluid. Most fluids contain ions, positive and negative . These ions interact with the object surface.
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 ...
They may also be responsible for the stabilization of colloidal suspension and will prevent particle aggregation of highly charged colloidal particles in aqueous suspensions. At low salt concentrations, the repulsive double layer forces can become rather long-ranged, and may lead to structuring of colloidal suspensions and eventually to ...
With an electrode, it is possible to regulate the surface charge by applying an external electric potential. This application, however, is impossible in colloidal and porous double layers, because for colloidal particles, one does not have access to the interior of the particle to apply a potential difference.
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.
Colloidal particles in water are typically charged, and there is an electrostatic potential, called a zeta potential at their surface. This charged surface of the colloidal particle interacts with a gradient in salt concentration, and this gives rise to diffusiophoretic velocity given by [3] [7]
The point of zero charge (pzc) is generally described as the pH at which the net electrical charge of the particle surface (i.e. adsorbent's surface) is equal to zero. This concept has been introduced in the studies dealing with colloidal flocculation to explain why pH is affecting the phenomenon.