Colloidal dispersions entropic stabilization

Electrically stabihzed colloidal dispersions are very sensitive to the addition of electrolytes. If the concentration of ions in the solution increases, decreases as a result of both entropic and electrical screening effects, leading to a reduction in the repulsive potential. On the other hand, colloid particles dispersed in organic media (low dielectric constant) cannot be effectively stabilized by charges because is extremely short. In these cases, steric stabilization is recommended. Steric stabihzation is imparted by nonionic amphiphilic molecules (usually polymeric molecules). The lyophobic moiety will adsorb onto the surface of the colloidal particles, while its lyophilic moiety will be extended in the continuous phase. When two sterically stabihzed particles approach each other, the concentration of the lyophilic segments in the portion of the continuous phase between the particles is increased. This higher local concentration results in an osmotic pressure that... 

Depletion force is expected to occur whenever nonadsorbing polymer is added to a colloidal dispersion. A polymer chain in solution will keep, on average, a configuration that is entropically most favorable. The polymer may approach a surface to a distance such that its farthest segments just meet the surface. To approach more closely, the polymer must adopt a less favorable conformation with a resulting loss of configurational entropy and also loss of system stability. 

The participation of colloidal particles in thermal motion (the entropic factor) was taken into consideration, mostly indirectly, in earlier studies dealing with the molecular-kinetic properties of disperse systems. Volmer was the first to realize the importance of the role that the thermal motion of colloidal particles played in controlling the formation and stabilization of disperse systems. However, the attempt to compare the work of surface formation and the entropic factor directly, undertaken by March, was not successful, since it was applied only to systems with high interfacial energy. 

Mixtures of clay platelets and polymer chains compose a colloidal system. Thus in the melt state, the propensity for the clay to be stably dispersed at the level of individual disks (an exfoliated clay dispersion) is dictated by clay, polymer, stabilizer, and compatibilizer potential interactions and the entropic effects of orientational disorder and confinement. An isometric dimension of clay platelets also has implications for stability because liquid crystalline phases may form. In addition, the very high melt viscosity of polypropylene and the colloidal size of clay imply slow particulate dynamics, thus equilibrium structures may be attained only very gradually. Agglomerated and networked clay structures may also lead to nonequilibrium behavior such as trapped states, aging, and glassy dynamics. 

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