GTU Questions
GTU Questions
GTU Questions
explain concept of DLVO theory with energy curves and how it can be applied
in colloidal dispersion stability ?
The well-known DLVO theory was established by Derjaguin, Landau, Verwey, and
Overbeek in the 1940s (Derjaguin and Landau 1941, Verwey and Overbeek 1948)
and describes the case where van der Waals forces are present in combination
with electrostatic forces. The theory is based on the assumption that the
electrostatic double layer forces and the van der Waals forces are independent and
therefore can be superimposed or added at each interacting distance for two
particles.
IN COLLOIDAL DISPERSION , BROWNIAN MOTION CAUSE FREQUENT COLLISIONS BETWEEN PARTICLES, SUCH ARE
RESPONSIBLE FOR THEIR Stability . 2 forces…
conclusions drawn..
STABILISATION
DLVO theory is a theory of colloidal dispersion stability in which zeta potential is used to explain
that as two particles approach one another their ionic atmospheres begin to overlap and a
repulsion force is developed.
Formation: Lyophilic colloids can be formed by adding the required substance to water. For
example, sugar can be added to water to form a lyophilic colloid. On the other hand, lyophobic
colloids are formed by adding the required substance to an organic solvent
settling: Lyophilic colloids do not settle out of solution even when left undisturbed. This is
because they are attracted to water molecules and remain suspended in the liquid. Lyophobic
colloids, on the other hand, will settle out of the solution if left undisturbed. This is because they
are not attracted to water molecules and will eventually fall to the bottom of the container
Particle Size: Lyophilic colloids tend to have larger particle sizes than lyophobic colloids.
This is because the particles are attracted to water molecules and can form large aggregates.
Lyophobic colloids, on the other hand, do not form large aggregates because the particles are not
attracted to each other
Stability: Lyophilic colloids are more stable than lyophobic colloids. This is because the
particles are attracted to water molecules and will not settle out of the solution, the dispersion
medium forms a solvent sheath around colloids making them thermodynamically stable.
Lyophobic colloids, on the other hand, are not as stable because the particles are not attracted to
each other and will settle out of the solution, there is charge present on particles (like) causing
uniformity due to repulsion become stable.
Affection from the heat: Lyophilic colloids are not affected by heat, while lyophobic colloids
are. This is because the particles in a lyophilic colloid are attracted to water molecules and will
not settle out of the solution even when heated. Lyophobic colloids, on the other hand, will settle
out of the solution when heated
Molecular Distribution: Lyophilic colloids have a more uniform distribution of molecules than
lyophobic colloids. This is because the particles are attracted to water molecules and will remain
suspended in the liquid. Lyophobic colloids, on the other hand, have a less uniform distribution
of molecules because the particles are not attracted to each other and will settle out of the
solution
Now you know the key differences between lyophilic and lyophobic colloids.
bottom of the container.
These molecules exhibit both lyophilic and
ASSOCIATION COLLOIDS:
lyophobic properties, certain affinity for both polar and non-polar
solvents. Association, or amphiphilic colloids are formed by the
grouping or self-association of the dispersed phase, which is
amphiphilic.
Here the head is polar part and the hydrocarbon chain is tail.
They are also called surface Active agents.
Micelle mech.
At low concentrations, amphiphiles exist separately as
(monomers subcolloidal in size) molecular dispersions or true
solutions which do not form a colloid. However, at higher
concentrations, self-association of several monomers, (monomer
aggregate themselves and are called as micelles) or
individual molecules occurs leading to micelle formation. Each
micelle may contain around 50 monomers and size may be about
50A. this size falls into colloidal range and are designated as
colloidal systems.
The formation of the micelles occurs above a particular
temperature called the Kraft temperature (Tk) and
The concentration at which micelles start forming is called
the critical micelle concentration. It is a range and has unit
such as w/w,
w/v %, moles/liter, moles/1000 g of solvent.
Below CMC, surfactants get absorbed on air water interface.
In this process, at one particular conc interface gets
saturated, while bulk phase is saturated with monomers.
The formation of micelles is spontaneous hence difficult to
differentiate the conc of saturated phase and micelle phase.
In bulk of soln, both are in dynamic equilibrium. This conc is
CMC. Beyond this addition increases the micelle formation.
Ionic surfactants have higher CMC than non-ionic
surfactants.
HLB value indicate that the surfactant is soluble in oil.
Selection of surfactants is important.
EXAMPLES: SLS(anionic), Cetyl trimethly ammonium
bromide(cationic), Polyoxyethylene Lauryl Ether(nonionic),
MECHANICAL SEPERATIO N
PREFRENTIAL CRYSTALLIZATION
BIOCHEMIC AL SEPERATIO N BY
DIASTEREO MERS
PRECIPITATION
CHROMATOGRAPHIC SEPERATION
KINETIC METHOD