INDEX Suspension stability

In soils and clays the most generally present biopolymers that naturally occur in the adsorbed state on mineral and clay particles are humic substances , or humic acids these are decomposition products of lignin, whidi is the major non-cellulosic polymer in wood and other plant debris. Humic acids (also called allomelanins (Merck Index, 1989)) are for the greater part polyphenolic compounds, usueJly anionic polyelectrolytes, which can complex metal ions, and are surface active and thus capable, upon adsorption onto mineral particles, to enhance their suspension stability in aqueous media (Chheda and Grasso, 1994). 

Figure 5 shows the calculated potential energy of interaction Vt of AI2O3 particles (t/ = 0.25 pm, A = 4.5 x 10 J, and 0.01 M ionic strength) as a function of the surface-to-surface distance of separation for various conditions of potential in an aqueous suspension. Note that the height of the potential energy barrier increases quite sharply as the potential becomes larger than a certain critical value ( 30 mV in Fig. 5). Therefore, the potential is a very good index of the magnitude of the repulsive interaction between colloid particles. Because of this, measurements of potential are most commonly used to assess the stability of a given colloidal sol.

From a knowledge of the adsorption, immersion, and wetting properties of solid particles, we have examined the influence of particle-particle and particle-liquid interactions on the stability and structure formation of suspensions of hydrophobic and hydrophilic Aerosil particles in benzene-n-heptane and methanol-benzene mixtures. For the binary mixtures, the Hamaker constants have been determined by optical dispersion measurements over the entire composition range by calculation of the characteristic frequency (Vk) from refractive index measurements [7,29,36,64], The Hamaker constant of an adsorption layer whose composition is different from that of the bulk has been calculated for several mixture compositions on the basis of the above results. Having the excess isotherms available enabled us to determine the adsorption layer thickness as a function of the mixture composition. For interparticle attractive potentials, calculations were done on the basis of the Vincent model [3-5,39]. In the case of hydrophobic particles dispersed in benzene- -heptane and methanol-benzene mixtures, it was established that the change in the attractive potential was in accordance with the interactions obtained from rheological measurements. 

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