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PREPARATION OF COLLOIDS

Lyophobic dispersions

The most common medium for lyophobic dispersion is water. Insoluble organic and inorganic compounds usually with a low degree of hydration are dispersed in aqueous medium and are intrinsically unstable. The particles tend to coalesce or aggregate to reduce the surface area and hence surface energy. Thus special means must be utilized to stabilize these systems –preventing the otherwise spontaneous coalescence or coagulation of the disperse phase after it has been finely dispersed. There are two methods of preparing lyophobic sols, namely Condensation methods (aggregation of small molecules or ions until particles of colloidal dimensions are obtained) and dispersion methods (reducing coarse particles to colloidal dimensions through comminution or peptization).

Condensation Method:

This method involves aggregation of small molecules or ions until particles of colloidal dimensions result.

To illustrate this method, the preparation of sulphur hydrosol is exemplified. Whereas sulphur is insoluble in water, it soluble in alcohol. Alcohol and water are miscible. Sulphur is dissolved in alcohol, and the solution is mixed with water to produce a bluish-white colloidal dispersion. The dispersion must be stabilized to avoid precipitation or agglomeration. The same method can be used to prepare hydrosol of stearic acid, mastic acid and other polymers.

Suphur vapor may also be stremed in water to produce a colloidal dispersion. This is a less common method.

Condensation may also be produced chemically. For example bubbling hydrogen sulphide (H2S) gas into a solution of sulphur dioxide (SO2) :



2H2S   +  SO2    ===>                       3S   +   H2O



or mixing solutions of sodium thiosulphate and sulfuric acid:


===>H2SO4 + 3NaS2O3                             4S +NaSO4 + H2O


Aluminium hydrxide sol is produced by hydrolysis of Aluminium chloride.

            AlCl3  +  3 H2O                          ===> Al(OH)3 + 3HCl                                


** See preparation of White lotion (precipitated ZnS and S)

Dispersion method:

The methods involve reducing coarse particles to colloidal dimensions through comminution or peptization.

Mechanical disintegration: 

Using equipment such as micronizers, colloid mills, homogenizers, or even simple mortar and pestle, solids and liquids are sheared or attrited into fine size for dispersion. Ultrasonic generators produce waves that break soft materials e.g. sulphur, talcum and graphite into very small particles or droplets. Thus method is used to produce very fine emulsions for I.V. use.

The dispersion must be stabilized to avoid re-crystallization, coagulation or calescence.

Peptization:

This involves breaking up aggregates into smaller particles. It is synonymous to defflocculation. It can be brought by removing flocculating agent (eg electrolyte) or addition of a deffloculating agents or peptizing agents (eg surfactants, ions or water soluble polymers). Eg activated charcoal produces a grey dispersion, Addition of 0.1% Na laurylsulphate or octoxynol disintegrates the particles into fine ones, results in fine deep black dispersion.  

Purification of colloidal dispersions

Hydrosols may contain low molecular weight water-soluble impurities including salts formed by reaction producing the dispersion. The salts tend to coagulate the dispersion and hence must be removed. Blood  ( a colloidal dispersion of plasma proteins) of patients with renal insufficiency has high concentration of urea and other metabolites. These as well must be removed to acceptable levels. Substances in true solutions may be separated from those in colloidal dispersion by means of dialysis or ultrafiltration.
Dialysis:

This is based upon the fact that colloidal particles do not diffuse (or diffuse very slowly) through membrane of parchment, cellophane, collodion or certain animal tissues, while particles of molecular or ionic dimensions diffuse relatively rapidly. Thus if  the low  molecular weight impurities are to be removed from a colloidal dispersion the latter is placed inside a sac made of one of the above mentioned membranes and dipped in water. The small solutes will diffuse out while pure colloidal materials are retained.

The rate of dialysis is increased increasing the area of membrane (e.g. using numerous hollow fibres, stirring and maintaining a high concentration gradient (dialysis fluid must be replenished continuously). If the impurities are electrolytes, the dialysis process can be speeded up by applying an electric potential to the sol. The process is then known as electrodialysis, and the equipment used is electrodialyser. Application of pressure in a dialytic process also speeds up the process. This is known as ultrafiltration.

Application of dialysis.

Dialysis is used in the laboratory to purify sols and study binding of drugs by proteins, as well as in some manufacturing process. The blood in uremic patients is dialysed  to remove urea, creatinine, uric acid, phosphates and other metabolites. The dialyzing fluids contain Na+, Cl- , KCl, Acetates, dextrose etc in same concentration as plasma. Urea, creatinine, uric acid, phosphates and other metabolites diffuse from blood side to dialysis fluid until their concentration equilibrates to that in blood. NaCl, KCl diffuse at initial high concentration until equilibrium. The volume of dialysis fluid is much higher than that of blood to ensure complete removal of unwanted metabolites and is continuously replenished. Plasma proteins and blood cells do not pass out because of their big size. Edema is relieved by vacuum pressure. The process is known as haemodialysis. It is also employed in cases of acute poisoning.