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Factors Affecting Solubility04:01

Factors Affecting Solubility

Compared with pure water, the solubility of an ionic compound is less in aqueous solutions containing a common ion (one also produced by dissolution of the ionic compound). This is an example of a phenomenon known as the common ion effect, which is a consequence of the law of mass action that may be explained using Le Chȃtelier’s principle. Consider the dissolution of silver iodide:
Coagulation01:06

Coagulation

Colloidal solids are solid particles suspended in solution. They are usually negatively charged, attracting a compact primary layer of positively charged ions, which attract more counterions to form an electrical double layer. Electrostatic repulsion between the charged double layers prevents the particles from colliding, stabilizing the colloids. These solids are often undesirable because they can contain toxins that are difficult to remove. Coagulation is a technique that helps aggregate and...
Colloidal precipitates01:09

Colloidal precipitates

The high insolubility of some precipitates can result in an unfavorable relative supersaturation. This can lead to colloidal particles with a large surface-to-mass ratio, where adsorption is promoted. For instance, in the precipitation of silver chloride, silver ions are adsorbed on the surface of the colloidal particles, forming a primary layer. This layer attracts ions of opposite charge (such as nitrate ions), forming a diffuse secondary layer of adsorbed ions. This electric double layer...
Ion Exchange01:17

Ion Exchange

Ion exchange chromatography separates charged molecules from a solution by reversibly exchanging them with mobile, or 'active', ions associated with the oppositely charged stationary phase. This method can be used to separate ions, soften and deionize water, and purify solutions. The polymers comprising the ion-exchange column are high-molecular-weight and chemically stable polymers, crosslinked to be porous and essentially insoluble. They are also functionalized with either acidic or basic...
Qualitative Analysis03:46

Qualitative Analysis

For solutions containing mixtures of different cations, the identity of each cation can be determined by qualitative analysis. This technique involves a series of selective precipitations with different chemical reagents, each reaction producing a characteristic precipitate for a specific group of cations. Metal ions within a group are further separated by varying the pH, heating the mixture to redissolve a precipitate, or adding other reagents to form complex ions.
For instance, group IV...
Ionic Strength: Effects on Chemical Equilibria01:19

Ionic Strength: Effects on Chemical Equilibria

The addition of an inert ionic compound increases the solubility of a sparingly soluble salt. For example, adding potassium nitrate to a saturated solution of calcium sulfate significantly enhances the solubility of calcium sulfate. Le Châtelier's principle cannot predict this shift in the equilibrium. Instead, this could be explained in terms of changes in the effective concentration of the ions in solution in the presence of added inert salt.
In this solution, the primary cation—the calcium...

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Related Experiment Video

Updated: May 19, 2026

Determination of the Settling Rate of Clay/Cyanobacterial Floccules
06:00

Determination of the Settling Rate of Clay/Cyanobacterial Floccules

Published on: June 11, 2018

Competition between kaolinite flocculation and stabilization in divalent cation solutions dosed with anionic

Byung Joon Lee1, Mark A Schlautman2, Erik Toorman3

  • 1Hydraulics Laboratory, Department of Civil Engineering, Katholieke University of Leuven, Kasteelpark Arenberg 40, B-3001 Heverlee, Belgium; Management Unit of the North Sea Mathematical Models (MUMM), Royal Belgian Institute of Natural Sciences, Gulledelle 100, 1200 Brussels, Belgium.

Water Research
|August 28, 2012
PubMed
Summary

Divalent cations like Ca(2+) and Mg(2+) can stabilize or destabilize colloidal particles, depending on how they bridge polyacrylamides (PAMs) and kaolinite. This study proposes a model explaining these dual effects in colloidal suspensions.

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Last Updated: May 19, 2026

Determination of the Settling Rate of Clay/Cyanobacterial Floccules
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Controlling the Size, Shape and Stability of Supramolecular Polymers in Water
16:24

Controlling the Size, Shape and Stability of Supramolecular Polymers in Water

Published on: August 2, 2012

Area of Science:

  • Colloid and Surface Science
  • Environmental Chemistry
  • Polymer Science

Background:

  • Divalent cations typically enhance flocculation by bridging anionic polyelectrolytes and colloidal particles.
  • However, stabilization effects have also been observed under certain conditions, necessitating further investigation.

Purpose of the Study:

  • To investigate the dual role of divalent cations (Ca(2+) and Mg(2+)) in the flocculation and stabilization of kaolinite suspensions with anionic polyacrylamides (PAMs).
  • To propose a conceptual model explaining the coexistence of flocculation and stabilization phenomena.

Main Methods:

  • Experimental study of kaolinite suspensions treated with various anionic polyacrylamides (PAMs).
  • Analysis of the effects of divalent cations (Ca(2+), Mg(2+)) on suspension stability and flocculation dynamics.

Main Results:

  • Divalent cations can induce both flocculation and stabilization in anionic PAM-kaolinite systems.
  • Particle-binding cationic bridges promote flocculation, while polymer-binding cationic bridges enhance steric stabilization.
  • Both bridging mechanisms coexist, leading to counteracting effects on colloidal stability.

Conclusions:

  • A conceptual model is proposed involving particle-binding and polymer-binding divalent cationic bridges.
  • Polymer-binding bridges can lead to colloid stabilization by forming protective polymer layers.
  • Anionic polyelectrolytes in divalent cation-rich solutions may stabilize colloidal particles via polymer-binding bridges.